Canonical Allele Identifier: CA625315099

Gene: MYO15A

Linked Data

• dbSNP Id: rs1334753372
• gnomAD v2: 17-18049159-G-A
• gnomAD v4: 17-18145845-G-A
• COSMIC: COSN19771510
• MyVariant Identifiers: chr17:g.18049159G>A (hg19) ; chr17:g.18145845G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18145845G>A , CM000679.2:g.18145845G>A	GRCh38
NC_000017.10:g.18049159G>A , CM000679.1:g.18049159G>A	GRCh37
NC_000017.9:g.17989884G>A	NCBI36
NG_011634.1:g.42140G>A
NG_011634.2:g.42140G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000647165.2:c.6274-27G>A MANE Select	ENSP00000495481.1:n.6274-27G>A
ENST00000205890.9:c.6274-27G>A	ENSP00000205890.5:n.6274-27G>A
ENST00000615845.4:c.6274-27G>A	ENSP00000481642.1:n.6274-27G>A
NM_016239.3:c.6274-27G>A	NP_057323.3:n.6274-27G>A
XM_011523917.1:c.6214-27G>A	XP_011522219.1:n.6214-27G>A
XM_011523918.1:c.6214-27G>A	XP_011522220.1:n.6214-27G>A
XM_011523921.1:c.6268-27G>A	XP_011522223.1:n.6268-27G>A
XR_934037.1:n.6873-27G>A
XR_934038.1:n.6873-27G>A
XM_011523918.2:c.6214-27G>A	XP_011522220.1:n.6214-27G>A
XM_017024714.2:c.6214-27G>A	XP_016880203.1:n.6214-27G>A
XM_017024715.2:c.6277-27G>A	XP_016880204.1:n.6277-27G>A
XM_024450781.1:c.6213+1253G>A	XP_024306549.1:n.6213+1253G>A
NM_016239.4:c.6274-27G>A MANE Select	NP_057323.3:n.6274-27G>A