Canonical Allele Identifier: CA406958795

Gene: MYH14

Linked Data

• MyVariant Identifiers: chr19:g.50789754A>G (hg19) ; chr19:g.50286497A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50286497A>G , CM000681.2:g.50286497A>G	GRCh38
NC_000019.9:g.50789754A>G , CM000681.1:g.50789754A>G	GRCh37
NC_000019.8:g.55481566A>G	NCBI36
NG_011645.1:g.87870A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000425460.6:c.4456A>G	ENSP00000407879.1:p.Lys1486Glu
ENST00000642316.2:c.4555A>G MANE Select	ENSP00000493594.1:p.Lys1519Glu
ENST00000262269.12:c.1444A>G	ENSP00000262269.9:p.Lys482Glu
ENST00000376970.6:c.4432A>G	ENSP00000366169.3:p.Lys1478Glu
ENST00000425460.5:c.4456A>G	ENSP00000407879.1:p.Lys1486Glu
ENST00000440075.6:c.361A>G	ENSP00000406273.3:p.Lys121Glu
ENST00000595016.1:n.1734A>G
ENST00000596571.5:c.4432A>G	ENSP00000472819.1:p.Lys1478Glu
ENST00000598205.5:c.4456A>G	ENSP00000472543.1:p.Lys1486Glu
ENST00000601313.5:c.4555A>G	ENSP00000470298.1:p.Lys1519Glu
NM_001077186.1:c.4456A>G	NP_001070654.1:p.Lys1486Glu
NM_001145809.1:c.4555A>G	NP_001139281.1:p.Lys1519Glu
NM_024729.3:c.4432A>G	NP_079005.3:p.Lys1478Glu
XM_006723386.2:c.4456A>G	XP_006723449.1:p.Lys1486Glu
XM_011527320.1:c.4576A>G	XP_011525622.1:p.Lys1526Glu
XM_011527321.1:c.4552A>G	XP_011525623.1:p.Lys1518Glu
XM_011527322.1:c.4480A>G	XP_011525624.1:p.Lys1494Glu
XM_011527323.1:c.4456A>G	XP_011525625.1:p.Lys1486Glu
XM_006723386.4:c.4456A>G	XP_006723449.1:p.Lys1486Glu
XM_011527320.2:c.4576A>G	XP_011525622.1:p.Lys1526Glu
XM_011527321.2:c.4552A>G	XP_011525623.1:p.Lys1518Glu
XM_011527323.2:c.4456A>G	XP_011525625.1:p.Lys1486Glu
XM_024451721.1:c.4432A>G	XP_024307489.1:p.Lys1478Glu
NM_001077186.2:c.4456A>G	NP_001070654.1:p.Lys1486Glu
NM_001145809.2:c.4555A>G MANE Select	NP_001139281.1:p.Lys1519Glu
NM_024729.4:c.4432A>G	NP_079005.3:p.Lys1478Glu