Canonical Allele Identifier: CA663260134

Gene: MYO3A

Linked Data

• dbSNP Id: rs1390316078
• MyVariant Identifiers: chr10:g.26501404C>T (hg19) ; chr10:g.26212475C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.26212475C>T , CM000672.2:g.26212475C>T	GRCh38
NC_000010.10:g.26501404C>T , CM000672.1:g.26501404C>T	GRCh37
NC_000010.9:g.26541410C>T	NCBI36
NG_011635.1:g.283403C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642920.2:c.*512C>T MANE Select	ENSP00000495965.1:n.*512C>T
ENST00000265944.9:c.*512C>T	ENSP00000265944.4:n.*512C>T
NM_017433.4:c.*512C>T	NP_059129.3:n.*512C>T
XM_011519498.1:c.*512C>T	XP_011517800.1:n.*512C>T
XM_011519499.1:c.*512C>T	XP_011517801.1:n.*512C>T
XM_011519500.1:c.*512C>T	XP_011517802.1:n.*512C>T
XM_011519501.1:c.*512C>T	XP_011517803.1:n.*512C>T
XM_011519504.1:c.*414C>T	XP_011517806.1:n.*414C>T
XM_011519505.1:c.*512C>T	XP_011517807.1:n.*512C>T
XM_011519507.1:c.*512C>T	XP_011517809.1:n.*512C>T
XM_011519512.1:c.*512C>T	XP_011517814.1:n.*512C>T
XM_011519513.1:c.*512C>T	XP_011517815.1:n.*512C>T
XR_930493.1:n.5460C>T
XM_011519498.2:c.*512C>T	XP_011517800.1:n.*512C>T
XM_011519500.2:c.*512C>T	XP_011517802.1:n.*512C>T
XM_011519513.2:c.*512C>T	XP_011517815.1:n.*512C>T
XR_001747111.1:n.4420C>T
NM_017433.5:c.*512C>T MANE Select	NP_059129.3:n.*512C>T