Canonical Allele Identifier: CA288407246
Gene: MYO15A HGNC NCBI

Linked Data

dbSNP Id: rs764109138
gnomAD v2: 17-18049036-C-CTA
gnomAD v3: 17-18145722-C-CTA
gnomAD v4: 17-18145722-C-CTA
MyVariant Identifiers: chr17:g.18049036_18049037insTA (hg19) chr17:g.18145722_18145723insTA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.18145731_18145732dup , CM000679.2:g.18145731_18145732dup GRCh38
NC_000017.10:g.18049045_18049046dup , CM000679.1:g.18049045_18049046dup GRCh37
NC_000017.9:g.17989770_17989771dup NCBI36
NG_011634.1:g.42026_42027dup
NG_011634.2:g.42026_42027dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000647165.2:c.6274-141_6274-140dup MANE Select ENSP00000495481.1:n.6274-141_6274-140dup
ENST00000205890.9:c.6274-141_6274-140dup ENSP00000205890.5:n.6274-141_6274-140dup
ENST00000615845.4:c.6274-141_6274-140dup ENSP00000481642.1:n.6274-141_6274-140dup
NM_016239.3:c.6274-141_6274-140dup NP_057323.3:n.6274-141_6274-140dup
XM_011523917.1:c.6214-141_6214-140dup XP_011522219.1:n.6214-141_6214-140dup
XM_011523918.1:c.6214-141_6214-140dup XP_011522220.1:n.6214-141_6214-140dup
XM_011523921.1:c.6268-141_6268-140dup XP_011522223.1:n.6268-141_6268-140dup
XR_934037.1:n.6873-141_6873-140dup
XR_934038.1:n.6873-141_6873-140dup
XM_011523918.2:c.6214-141_6214-140dup XP_011522220.1:n.6214-141_6214-140dup
XM_017024714.2:c.6214-141_6214-140dup XP_016880203.1:n.6214-141_6214-140dup
XM_017024715.2:c.6277-141_6277-140dup XP_016880204.1:n.6277-141_6277-140dup
XM_024450781.1:c.6213+1139_6213+1140dup XP_024306549.1:n.6213+1139_6213+1140dup
NM_016239.4:c.6274-141_6274-140dup MANE Select NP_057323.3:n.6274-141_6274-140dup
Search 100 bp 5'
Search 100 bp 3'