Canonical Allele Identifier: CA2340825576

Gene: MYH14

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50286649T= , CM000681.2:g.50286649T=	GRCh38
NC_000019.9:g.50789906T= , CM000681.1:g.50789906T=	GRCh37
NC_000019.8:g.55481718T=	NCBI36
NG_011645.1:g.88022T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000425460.6:c.4608T=	ENSP00000407879.1:p.Ala1536=
ENST00000642316.2:c.4707T= MANE Select	ENSP00000493594.1:p.Ala1569=
ENST00000262269.12:c.*68T=	ENSP00000262269.9:n.*68T=
ENST00000376970.6:c.4584T=	ENSP00000366169.3:p.Ala1528=
ENST00000425460.5:c.4608T=	ENSP00000407879.1:p.Ala1536=
ENST00000440075.6:c.513T=	ENSP00000406273.3:p.Ala171=
ENST00000595016.1:n.1886T=
ENST00000596571.5:c.4584T=	ENSP00000472819.1:p.Ala1528=
ENST00000598205.5:c.4608T=	ENSP00000472543.1:p.Ala1536=
ENST00000601313.5:c.4707T=	ENSP00000470298.1:p.Ala1569=
NM_001077186.1:c.4608T=	NP_001070654.1:p.Ala1536=
NM_001145809.1:c.4707T=	NP_001139281.1:p.Ala1569=
NM_024729.3:c.4584T=	NP_079005.3:p.Ala1528=
XM_006723386.2:c.4608T=	XP_006723449.1:p.Ala1536=
XM_011527320.1:c.4728T=	XP_011525622.1:p.Ala1576=
XM_011527321.1:c.4704T=	XP_011525623.1:p.Ala1568=
XM_011527322.1:c.4632T=	XP_011525624.1:p.Ala1544=
XM_011527323.1:c.4608T=	XP_011525625.1:p.Ala1536=
XM_006723386.4:c.4608T=	XP_006723449.1:p.Ala1536=
XM_011527320.2:c.4728T=	XP_011525622.1:p.Ala1576=
XM_011527321.2:c.4704T=	XP_011525623.1:p.Ala1568=
XM_011527323.2:c.4608T=	XP_011525625.1:p.Ala1536=
XM_024451721.1:c.4584T=	XP_024307489.1:p.Ala1528=
NM_001077186.2:c.4608T=	NP_001070654.1:p.Ala1536=
NM_001145809.2:c.4707T= MANE Select	NP_001139281.1:p.Ala1569=
NM_024729.4:c.4584T=	NP_079005.3:p.Ala1528=