Canonical Allele Identifier: CA2466571556
Gene: MECP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154032297_154032301delinsTCATA , CM000685.2:g.154032297_154032301delinsTCATA GRCh38
NC_000023.10:g.153297748_153297752delinsTCATA , CM000685.1:g.153297748_153297752delinsTCATA GRCh37
NC_000023.9:g.152950942_152950946delinsTCATA NCBI36
NG_007107.2:g.109827_109831delinsTATGA
NG_007107.3:g.109803_109807delinsTATGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000303391.11:c.283_287delinsTATGA MANE Plus Clinical ENSP00000301948.6:p.Tyr95=
ENST00000453960.7:c.319_323delinsTATGA MANE Select ENSP00000395535.2:p.Tyr107=
ENST00000303391.10:c.283_287delinsTATGA ENSP00000301948.6:p.Tyr95=
ENST00000369957.5:c.*337_*341delinsTATGA ENSP00000358973.4:n.*337_*341delinsTATGA
ENST00000407218.5:c.319_323delinsTATGA ENSP00000384865.2:p.Tyr107=
ENST00000453960.6:c.319_323delinsTATGA ENSP00000395535.2:p.Tyr107=
ENST00000486506.5:n.2631_2635delinsTATGA
ENST00000611468.1:c.271_275delinsTATGA ENSP00000479736.1:p.Tyr91=
ENST00000619732.4:c.283_287delinsTATGA ENSP00000480973.1:p.Tyr95=
ENST00000622433.4:c.271_275delinsTATGA ENSP00000484470.1:p.Tyr91=
ENST00000628176.2:c.283_287delinsTATGA ENSP00000486978.1:p.Tyr95=
NM_001110792.1:c.319_323delinsTATGA NP_001104262.1:p.Tyr107=
NM_001316337.1:c.4_8delinsTATGA NP_001303266.1:p.Tyr2=
NM_004992.3:c.283_287delinsTATGA NP_004983.1:p.Tyr95=
XM_005274681.3:c.283_287delinsTATGA XP_005274738.1:p.Tyr95=
XM_005274682.3:c.4_8delinsTATGA XP_005274739.1:p.Tyr2=
XM_005274683.3:c.4_8delinsTATGA XP_005274740.1:p.Tyr2=
XM_011531166.1:c.4_8delinsTATGA XP_011529468.1:p.Tyr2=
XM_006724819.3:c.-278_-274delinsTATGA XP_006724882.1:n.-278_-274delinsTATGA
XM_011531166.2:c.4_8delinsTATGA XP_011529468.1:p.Tyr2=
XM_024452383.1:c.4_8delinsTATGA XP_024308151.1:p.Tyr2=
XM_024452384.1:c.4_8delinsTATGA XP_024308152.1:p.Tyr2=
NM_001110792.2:c.319_323delinsTATGA MANE Select NP_001104262.1:p.Tyr107=
NM_001316337.2:c.4_8delinsTATGA NP_001303266.1:p.Tyr2=
NM_001369391.2:c.4_8delinsTATGA NP_001356320.1:p.Tyr2=
NM_001369392.2:c.4_8delinsTATGA NP_001356321.1:p.Tyr2=
NM_001369393.2:c.4_8delinsTATGA NP_001356322.1:p.Tyr2=
NM_001369394.1:c.4_8delinsTATGA NP_001356323.1:p.Tyr2=
NM_001369394.2:c.4_8delinsTATGA NP_001356323.1:p.Tyr2=
NM_001386137.1:c.-278_-274delinsTATGA NP_001373066.1:n.-278_-274delinsTATGA
NM_001386138.1:c.-278_-274delinsTATGA NP_001373067.1:n.-278_-274delinsTATGA
NM_001386139.1:c.-278_-274delinsTATGA NP_001373068.1:n.-278_-274delinsTATGA
NM_004992.4:c.283_287delinsTATGA MANE Plus Clinical NP_004983.1:p.Tyr95=