Canonical Allele Identifier: CA2340790530

Gene: MYH14

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50210631T= , CM000681.2:g.50210631T=	GRCh38
NC_000019.9:g.50713888T= , CM000681.1:g.50713888T=	GRCh37
NC_000019.8:g.55405700T=	NCBI36
NG_011645.1:g.12004T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000425460.6:c.266T=	ENSP00000407879.1:p.Leu89=
ENST00000642316.2:c.266T= MANE Select	ENSP00000493594.1:p.Leu89=
ENST00000642980.1:c.266T=	ENSP00000493650.1:p.Leu89=
ENST00000646861.1:c.266T=	ENSP00000493667.1:p.Leu89=
ENST00000376970.6:c.266T=	ENSP00000366169.3:p.Leu89=
ENST00000425460.5:c.266T=	ENSP00000407879.1:p.Leu89=
ENST00000440075.6:c.-2025T=	ENSP00000406273.3:n.-2025T=
ENST00000596571.5:c.266T=	ENSP00000472819.1:p.Leu89=
ENST00000598205.5:c.266T=	ENSP00000472543.1:p.Leu89=
ENST00000599920.5:c.266T=	ENSP00000469573.1:p.Leu89=
ENST00000601313.5:c.266T=	ENSP00000470298.1:p.Leu89=
NM_001077186.1:c.266T=	NP_001070654.1:p.Leu89=
NM_001145809.1:c.266T=	NP_001139281.1:p.Leu89=
NM_024729.3:c.266T=	NP_079005.3:p.Leu89=
XM_006723386.2:c.266T=	XP_006723449.1:p.Leu89=
XM_011527320.1:c.386T=	XP_011525622.1:p.Leu129=
XM_011527321.1:c.386T=	XP_011525623.1:p.Leu129=
XM_011527322.1:c.386T=	XP_011525624.1:p.Leu129=
XM_011527323.1:c.266T=	XP_011525625.1:p.Leu89=
XM_006723386.4:c.266T=	XP_006723449.1:p.Leu89=
XM_011527320.2:c.386T=	XP_011525622.1:p.Leu129=
XM_011527321.2:c.386T=	XP_011525623.1:p.Leu129=
XM_011527323.2:c.266T=	XP_011525625.1:p.Leu89=
XM_024451721.1:c.266T=	XP_024307489.1:p.Leu89=
NM_001077186.2:c.266T=	NP_001070654.1:p.Leu89=
NM_001145809.2:c.266T= MANE Select	NP_001139281.1:p.Leu89=
NM_024729.4:c.266T=	NP_079005.3:p.Leu89=