Canonical Allele Identifier: CA204337827

Gene: MYO3A

Linked Data

• ClinVar Variation Id: 879708
• ClinVar RCV Id: RCV001107410
• dbSNP Id: rs929411495
• gnomAD v2: 10-26223216-G-A
• gnomAD v3: 10-25934287-G-A
• gnomAD v4: 10-25934287-G-A
• MyVariant Identifiers: chr10:g.26223216G>A (hg19) ; chr10:g.25934287G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.25934287G>A , CM000672.2:g.25934287G>A	GRCh38
NC_000010.10:g.26223216G>A , CM000672.1:g.26223216G>A	GRCh37
NC_000010.9:g.26263222G>A	NCBI36
NG_011635.1:g.5215G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642197.1:n.59G>A
ENST00000642920.2:c.-146G>A MANE Select	ENSP00000495965.1:n.-146G>A
ENST00000265944.9:c.-146G>A	ENSP00000265944.4:n.-146G>A
ENST00000376302.5:c.-146G>A	ENSP00000365479.1:n.-146G>A
NM_017433.4:c.-146G>A	NP_059129.3:n.-146G>A
XM_011519500.1:c.-203G>A	XP_011517802.1:n.-203G>A
XM_011519501.1:c.-59G>A	XP_011517803.1:n.-59G>A
XM_011519502.1:c.-146G>A	XP_011517804.1:n.-146G>A
XM_011519503.1:c.-146G>A	XP_011517805.1:n.-146G>A
XM_011519504.1:c.-146G>A	XP_011517806.1:n.-146G>A
XM_011519505.1:c.-146G>A	XP_011517807.1:n.-146G>A
XM_011519506.1:c.-146G>A	XP_011517808.1:n.-146G>A
XM_011519508.1:c.-146G>A	XP_011517810.1:n.-146G>A
XM_011519509.1:c.-146G>A	XP_011517811.1:n.-146G>A
XM_011519510.1:c.-146G>A	XP_011517812.1:n.-146G>A
XM_011519511.1:c.-146G>A	XP_011517813.1:n.-146G>A
XR_930492.1:n.59G>A
XR_930493.1:n.59G>A
XR_930494.1:n.59G>A
XM_011519500.2:c.-203G>A	XP_011517802.1:n.-203G>A
XM_011519506.2:c.-146G>A	XP_011517808.1:n.-146G>A
XM_011519508.2:c.-146G>A	XP_011517810.1:n.-146G>A
XM_011519510.2:c.-146G>A	XP_011517812.1:n.-146G>A
XM_011519511.2:c.-146G>A	XP_011517813.1:n.-146G>A
XR_001747111.1:n.59G>A
NM_017433.5:c.-146G>A MANE Select	NP_059129.3:n.-146G>A
NM_001368265.1:c.-146G>A	NP_001355194.1:n.-146G>A