Canonical Allele Identifier: CA663260064

Gene: MYO3A

Linked Data

• dbSNP Id: rs1277741656
• gnomAD v3: 10-26212371-C-T
• gnomAD v4: 10-26212371-C-T
• MyVariant Identifiers: chr10:g.26501300C>T (hg19) ; chr10:g.26212371C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.26212371C>T , CM000672.2:g.26212371C>T	GRCh38
NC_000010.10:g.26501300C>T , CM000672.1:g.26501300C>T	GRCh37
NC_000010.9:g.26541306C>T	NCBI36
NG_011635.1:g.283299C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642920.2:c.*408C>T MANE Select	ENSP00000495965.1:n.*408C>T
ENST00000645292.1:n.719C>T
ENST00000265944.9:c.*408C>T	ENSP00000265944.4:n.*408C>T
NM_017433.4:c.*408C>T	NP_059129.3:n.*408C>T
XM_011519498.1:c.*408C>T	XP_011517800.1:n.*408C>T
XM_011519499.1:c.*408C>T	XP_011517801.1:n.*408C>T
XM_011519500.1:c.*408C>T	XP_011517802.1:n.*408C>T
XM_011519501.1:c.*408C>T	XP_011517803.1:n.*408C>T
XM_011519504.1:c.*310C>T	XP_011517806.1:n.*310C>T
XM_011519505.1:c.*408C>T	XP_011517807.1:n.*408C>T
XM_011519507.1:c.*408C>T	XP_011517809.1:n.*408C>T
XM_011519512.1:c.*408C>T	XP_011517814.1:n.*408C>T
XM_011519513.1:c.*408C>T	XP_011517815.1:n.*408C>T
XR_930493.1:n.5356C>T
XM_011519498.2:c.*408C>T	XP_011517800.1:n.*408C>T
XM_011519500.2:c.*408C>T	XP_011517802.1:n.*408C>T
XM_011519513.2:c.*408C>T	XP_011517815.1:n.*408C>T
XR_001747111.1:n.4316C>T
NM_017433.5:c.*408C>T MANE Select	NP_059129.3:n.*408C>T