Canonical Allele Identifier: CA406958799

Gene: MYH14

Linked Data

• MyVariant Identifiers: chr19:g.50789755A>T (hg19) ; chr19:g.50286498A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50286498A>T , CM000681.2:g.50286498A>T	GRCh38
NC_000019.9:g.50789755A>T , CM000681.1:g.50789755A>T	GRCh37
NC_000019.8:g.55481567A>T	NCBI36
NG_011645.1:g.87871A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000425460.6:c.4457A>T	ENSP00000407879.1:p.Lys1486Met
ENST00000642316.2:c.4556A>T MANE Select	ENSP00000493594.1:p.Lys1519Met
ENST00000262269.12:c.1445A>T	ENSP00000262269.9:p.Lys482Met
ENST00000376970.6:c.4433A>T	ENSP00000366169.3:p.Lys1478Met
ENST00000425460.5:c.4457A>T	ENSP00000407879.1:p.Lys1486Met
ENST00000440075.6:c.362A>T	ENSP00000406273.3:p.Lys121Met
ENST00000595016.1:n.1735A>T
ENST00000596571.5:c.4433A>T	ENSP00000472819.1:p.Lys1478Met
ENST00000598205.5:c.4457A>T	ENSP00000472543.1:p.Lys1486Met
ENST00000601313.5:c.4556A>T	ENSP00000470298.1:p.Lys1519Met
NM_001077186.1:c.4457A>T	NP_001070654.1:p.Lys1486Met
NM_001145809.1:c.4556A>T	NP_001139281.1:p.Lys1519Met
NM_024729.3:c.4433A>T	NP_079005.3:p.Lys1478Met
XM_006723386.2:c.4457A>T	XP_006723449.1:p.Lys1486Met
XM_011527320.1:c.4577A>T	XP_011525622.1:p.Lys1526Met
XM_011527321.1:c.4553A>T	XP_011525623.1:p.Lys1518Met
XM_011527322.1:c.4481A>T	XP_011525624.1:p.Lys1494Met
XM_011527323.1:c.4457A>T	XP_011525625.1:p.Lys1486Met
XM_006723386.4:c.4457A>T	XP_006723449.1:p.Lys1486Met
XM_011527320.2:c.4577A>T	XP_011525622.1:p.Lys1526Met
XM_011527321.2:c.4553A>T	XP_011525623.1:p.Lys1518Met
XM_011527323.2:c.4457A>T	XP_011525625.1:p.Lys1486Met
XM_024451721.1:c.4433A>T	XP_024307489.1:p.Lys1478Met
NM_001077186.2:c.4457A>T	NP_001070654.1:p.Lys1486Met
NM_001145809.2:c.4556A>T MANE Select	NP_001139281.1:p.Lys1519Met
NM_024729.4:c.4433A>T	NP_079005.3:p.Lys1478Met