Canonical Allele Identifier: CA2608578934

Gene: MYO3A

Linked Data

• gnomAD v4: 10-26212238-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.26212238G>A , CM000672.2:g.26212238G>A	GRCh38
NC_000010.10:g.26501167G>A , CM000672.1:g.26501167G>A	GRCh37
NC_000010.9:g.26541173G>A	NCBI36
NG_011635.1:g.283166G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642920.2:c.*275G>A MANE Select	ENSP00000495965.1:n.*275G>A
ENST00000644253.1:n.792G>A
ENST00000645292.1:n.586G>A
ENST00000265944.9:c.*275G>A	ENSP00000265944.4:n.*275G>A
NM_017433.4:c.*275G>A	NP_059129.3:n.*275G>A
XM_011519498.1:c.*275G>A	XP_011517800.1:n.*275G>A
XM_011519499.1:c.*275G>A	XP_011517801.1:n.*275G>A
XM_011519500.1:c.*275G>A	XP_011517802.1:n.*275G>A
XM_011519501.1:c.*275G>A	XP_011517803.1:n.*275G>A
XM_011519504.1:c.*177G>A	XP_011517806.1:n.*177G>A
XM_011519505.1:c.*275G>A	XP_011517807.1:n.*275G>A
XM_011519507.1:c.*275G>A	XP_011517809.1:n.*275G>A
XM_011519512.1:c.*275G>A	XP_011517814.1:n.*275G>A
XM_011519513.1:c.*275G>A	XP_011517815.1:n.*275G>A
XR_930493.1:n.5223G>A
XM_011519498.2:c.*275G>A	XP_011517800.1:n.*275G>A
XM_011519500.2:c.*275G>A	XP_011517802.1:n.*275G>A
XM_011519513.2:c.*275G>A	XP_011517815.1:n.*275G>A
XR_001747111.1:n.4183G>A
NM_017433.5:c.*275G>A MANE Select	NP_059129.3:n.*275G>A