Canonical Allele Identifier: CA398604022
Gene: MYO15A HGNC NCBI

Linked Data

dbSNP Id: rs968618534
MyVariant Identifiers: chr17:g.18046155G>A (hg19) chr17:g.18142841G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.18142841G>A , CM000679.2:g.18142841G>A GRCh38
NC_000017.10:g.18046155G>A , CM000679.1:g.18046155G>A GRCh37
NC_000017.9:g.17986880G>A NCBI36
NG_011634.1:g.39136G>A
NG_011634.2:g.39136G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000647165.2:c.5910+1G>A MANE Select ENSP00000495481.1:n.5910+1G>A
ENST00000205890.9:c.5910+1G>A ENSP00000205890.5:n.5910+1G>A
ENST00000615845.4:c.5910+1G>A ENSP00000481642.1:n.5910+1G>A
NM_016239.3:c.5910+1G>A NP_057323.3:n.5910+1G>A
XM_011523917.1:c.5904+1G>A XP_011522219.1:n.5904+1G>A
XM_011523918.1:c.5904+1G>A XP_011522220.1:n.5904+1G>A
XM_011523919.1:c.5904+1G>A XP_011522221.1:n.5904+1G>A
XM_011523920.1:c.5904+1G>A XP_011522222.1:n.5904+1G>A
XM_011523921.1:c.5904+1G>A XP_011522223.1:n.5904+1G>A
XR_934037.1:n.6563+1G>A
XR_934038.1:n.6563+1G>A
XR_934039.1:n.6563+1G>A
XM_011523918.2:c.5904+1G>A XP_011522220.1:n.5904+1G>A
XM_017024714.2:c.5904+1G>A XP_016880203.1:n.5904+1G>A
XM_017024715.2:c.5913+1G>A XP_016880204.1:n.5913+1G>A
XM_024450780.1:c.5904+1G>A XP_024306548.1:n.5904+1G>A
XM_024450781.1:c.5904+1G>A XP_024306549.1:n.5904+1G>A
XM_024450782.1:c.5904+1G>A XP_024306550.1:n.5904+1G>A
XR_934039.2:n.6602+1G>A
NM_016239.4:c.5910+1G>A MANE Select NP_057323.3:n.5910+1G>A
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