Canonical Allele Identifier: CA9593561
Gene: MYH14 HGNC NCBI

Linked Data

ClinVar Variation Id: 505306
dbSNP Id: rs375866139

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50286559T>G , CM000681.2:g.50286559T>G GRCh38
NC_000019.9:g.50789816T>G , CM000681.1:g.50789816T>G GRCh37
NC_000019.8:g.55481628T>G NCBI36
NG_011645.1:g.87932T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000425460.6:c.4518T>G ENSP00000407879.1:p.Arg1506=
ENST00000642316.2:c.4617T>G MANE Select ENSP00000493594.1:p.Arg1539=
ENST00000262269.12:c.1505T>G ENSP00000262269.9:p.Val502Gly
ENST00000376970.6:c.4494T>G ENSP00000366169.3:p.Arg1498=
ENST00000425460.5:c.4518T>G ENSP00000407879.1:p.Arg1506=
ENST00000440075.6:c.423T>G ENSP00000406273.3:p.Arg141=
ENST00000595016.1:n.1796T>G
ENST00000596571.5:n.4494T>G ENSP00000472819.1:p.Arg1498=
ENST00000598205.5:c.4518T>G ENSP00000472543.1:p.Arg1506=
ENST00000601313.5:c.4617T>G ENSP00000470298.1:p.Arg1539=
NM_001077186.1:c.4518T>G NP_001070654.1:p.Arg1506=
NM_001145809.1:c.4617T>G NP_001139281.1:p.Arg1539=
NM_024729.3:c.4494T>G NP_079005.3:p.Arg1498=
XM_006723386.2:c.4518T>G XP_006723449.1:p.Arg1506=
XM_011527320.1:c.4638T>G XP_011525622.1:p.Arg1546=
XM_011527321.1:c.4614T>G XP_011525623.1:p.Arg1538=
XM_011527322.1:c.4542T>G XP_011525624.1:p.Arg1514=
XM_011527323.1:c.4518T>G XP_011525625.1:p.Arg1506=
XM_006723386.4:c.4518T>G XP_006723449.1:p.Arg1506=
XM_011527320.2:c.4638T>G XP_011525622.1:p.Arg1546=
XM_011527321.2:c.4614T>G XP_011525623.1:p.Arg1538=
XM_011527323.2:c.4518T>G XP_011525625.1:p.Arg1506=
XM_024451721.1:c.4494T>G XP_024307489.1:p.Arg1498=
NM_001077186.2:c.4518T>G NP_001070654.1:p.Arg1506=
NM_001145809.2:c.4617T>G MANE Select NP_001139281.1:p.Arg1539=
NM_024729.4:c.4494T>G NP_079005.3:p.Arg1498=