Canonical Allele Identifier: CA2340817265

Gene: MYH14

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50268319C= , CM000681.2:g.50268319C=	GRCh38
NC_000019.9:g.50771576C= , CM000681.1:g.50771576C=	GRCh37
NC_000019.8:g.55463388C=	NCBI36
NG_011645.1:g.69692C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000425460.6:c.2886C=	ENSP00000407879.1:p.Cys962=
ENST00000642316.2:c.2985C= MANE Select	ENSP00000493594.1:p.Cys995=
ENST00000376970.6:c.2862C=	ENSP00000366169.3:p.Cys954=
ENST00000425460.5:c.2886C=	ENSP00000407879.1:p.Cys962=
ENST00000440075.6:c.-727-7672C=	ENSP00000406273.3:n.-727-7672C=
ENST00000596571.5:c.2862C=	ENSP00000472819.1:p.Cys954=
ENST00000598205.5:c.2886C=	ENSP00000472543.1:p.Cys962=
ENST00000599920.5:c.2886C=	ENSP00000469573.1:p.Cys962=
ENST00000601313.5:c.2985C=	ENSP00000470298.1:p.Cys995=
NM_001077186.1:c.2886C=	NP_001070654.1:p.Cys962=
NM_001145809.1:c.2985C=	NP_001139281.1:p.Cys995=
NM_024729.3:c.2862C=	NP_079005.3:p.Cys954=
XM_006723386.2:c.2886C=	XP_006723449.1:p.Cys962=
XM_011527320.1:c.3006C=	XP_011525622.1:p.Cys1002=
XM_011527321.1:c.2982C=	XP_011525623.1:p.Cys994=
XM_011527322.1:c.2910C=	XP_011525624.1:p.Cys970=
XM_011527323.1:c.2886C=	XP_011525625.1:p.Cys962=
XM_006723386.4:c.2886C=	XP_006723449.1:p.Cys962=
XM_011527320.2:c.3006C=	XP_011525622.1:p.Cys1002=
XM_011527321.2:c.2982C=	XP_011525623.1:p.Cys994=
XM_011527323.2:c.2886C=	XP_011525625.1:p.Cys962=
XM_024451721.1:c.2862C=	XP_024307489.1:p.Cys954=
NM_001077186.2:c.2886C=	NP_001070654.1:p.Cys962=
NM_001145809.2:c.2985C= MANE Select	NP_001139281.1:p.Cys995=
NM_024729.4:c.2862C=	NP_079005.3:p.Cys954=