Canonical Allele Identifier: CA2340817270

Gene: MYH14

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50268329A= , CM000681.2:g.50268329A=	GRCh38
NC_000019.9:g.50771586A= , CM000681.1:g.50771586A=	GRCh37
NC_000019.8:g.55463398A=	NCBI36
NG_011645.1:g.69702A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000425460.6:c.2896A=	ENSP00000407879.1:p.Met966=
ENST00000642316.2:c.2995A= MANE Select	ENSP00000493594.1:p.Met999=
ENST00000376970.6:c.2872A=	ENSP00000366169.3:p.Met958=
ENST00000425460.5:c.2896A=	ENSP00000407879.1:p.Met966=
ENST00000440075.6:c.-727-7662A=	ENSP00000406273.3:n.-727-7662A=
ENST00000596571.5:c.2872A=	ENSP00000472819.1:p.Met958=
ENST00000598205.5:c.2896A=	ENSP00000472543.1:p.Met966=
ENST00000599920.5:c.2896A=	ENSP00000469573.1:p.Met966=
ENST00000601313.5:c.2995A=	ENSP00000470298.1:p.Met999=
NM_001077186.1:c.2896A=	NP_001070654.1:p.Met966=
NM_001145809.1:c.2995A=	NP_001139281.1:p.Met999=
NM_024729.3:c.2872A=	NP_079005.3:p.Met958=
XM_006723386.2:c.2896A=	XP_006723449.1:p.Met966=
XM_011527320.1:c.3016A=	XP_011525622.1:p.Met1006=
XM_011527321.1:c.2992A=	XP_011525623.1:p.Met998=
XM_011527322.1:c.2920A=	XP_011525624.1:p.Met974=
XM_011527323.1:c.2896A=	XP_011525625.1:p.Met966=
XM_006723386.4:c.2896A=	XP_006723449.1:p.Met966=
XM_011527320.2:c.3016A=	XP_011525622.1:p.Met1006=
XM_011527321.2:c.2992A=	XP_011525623.1:p.Met998=
XM_011527323.2:c.2896A=	XP_011525625.1:p.Met966=
XM_024451721.1:c.2872A=	XP_024307489.1:p.Met958=
NM_001077186.2:c.2896A=	NP_001070654.1:p.Met966=
NM_001145809.2:c.2995A= MANE Select	NP_001139281.1:p.Met999=
NM_024729.4:c.2872A=	NP_079005.3:p.Met958=