Canonical Allele Identifier: CA2608579048

Gene: MYO3A

Linked Data

• gnomAD v4: 10-26212369-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.26212369A>C , CM000672.2:g.26212369A>C	GRCh38
NC_000010.10:g.26501298A>C , CM000672.1:g.26501298A>C	GRCh37
NC_000010.9:g.26541304A>C	NCBI36
NG_011635.1:g.283297A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642920.2:c.*406A>C MANE Select	ENSP00000495965.1:n.*406A>C
ENST00000645292.1:n.717A>C
ENST00000265944.9:c.*406A>C	ENSP00000265944.4:n.*406A>C
NM_017433.4:c.*406A>C	NP_059129.3:n.*406A>C
XM_011519498.1:c.*406A>C	XP_011517800.1:n.*406A>C
XM_011519499.1:c.*406A>C	XP_011517801.1:n.*406A>C
XM_011519500.1:c.*406A>C	XP_011517802.1:n.*406A>C
XM_011519501.1:c.*406A>C	XP_011517803.1:n.*406A>C
XM_011519504.1:c.*308A>C	XP_011517806.1:n.*308A>C
XM_011519505.1:c.*406A>C	XP_011517807.1:n.*406A>C
XM_011519507.1:c.*406A>C	XP_011517809.1:n.*406A>C
XM_011519512.1:c.*406A>C	XP_011517814.1:n.*406A>C
XM_011519513.1:c.*406A>C	XP_011517815.1:n.*406A>C
XR_930493.1:n.5354A>C
XM_011519498.2:c.*406A>C	XP_011517800.1:n.*406A>C
XM_011519500.2:c.*406A>C	XP_011517802.1:n.*406A>C
XM_011519513.2:c.*406A>C	XP_011517815.1:n.*406A>C
XR_001747111.1:n.4314A>C
NM_017433.5:c.*406A>C MANE Select	NP_059129.3:n.*406A>C