Canonical Allele Identifier: CA926095136

Gene: MYO3A

Linked Data

• dbSNP Id: rs1844266943
• gnomAD v3: 10-26212363-A-T
• gnomAD v4: 10-26212363-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.26212363A>T , CM000672.2:g.26212363A>T	GRCh38
NC_000010.10:g.26501292A>T , CM000672.1:g.26501292A>T	GRCh37
NC_000010.9:g.26541298A>T	NCBI36
NG_011635.1:g.283291A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642920.2:c.*400A>T MANE Select	ENSP00000495965.1:n.*400A>T
ENST00000645292.1:n.711A>T
ENST00000265944.9:c.*400A>T	ENSP00000265944.4:n.*400A>T
NM_017433.4:c.*400A>T	NP_059129.3:n.*400A>T
XM_011519498.1:c.*400A>T	XP_011517800.1:n.*400A>T
XM_011519499.1:c.*400A>T	XP_011517801.1:n.*400A>T
XM_011519500.1:c.*400A>T	XP_011517802.1:n.*400A>T
XM_011519501.1:c.*400A>T	XP_011517803.1:n.*400A>T
XM_011519504.1:c.*302A>T	XP_011517806.1:n.*302A>T
XM_011519505.1:c.*400A>T	XP_011517807.1:n.*400A>T
XM_011519507.1:c.*400A>T	XP_011517809.1:n.*400A>T
XM_011519512.1:c.*400A>T	XP_011517814.1:n.*400A>T
XM_011519513.1:c.*400A>T	XP_011517815.1:n.*400A>T
XR_930493.1:n.5348A>T
XM_011519498.2:c.*400A>T	XP_011517800.1:n.*400A>T
XM_011519500.2:c.*400A>T	XP_011517802.1:n.*400A>T
XM_011519513.2:c.*400A>T	XP_011517815.1:n.*400A>T
XR_001747111.1:n.4308A>T
NM_017433.5:c.*400A>T MANE Select	NP_059129.3:n.*400A>T