Canonical Allele Identifier: CA406958762

Gene: MYH14

Linked Data

• MyVariant Identifiers: chr19:g.50789739C>G (hg19) ; chr19:g.50286482C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50286482C>G , CM000681.2:g.50286482C>G	GRCh38
NC_000019.9:g.50789739C>G , CM000681.1:g.50789739C>G	GRCh37
NC_000019.8:g.55481551C>G	NCBI36
NG_011645.1:g.87855C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000425460.6:c.4441C>G	ENSP00000407879.1:p.Leu1481Val
ENST00000642316.2:c.4540C>G MANE Select	ENSP00000493594.1:p.Leu1514Val
ENST00000262269.12:c.1429C>G	ENSP00000262269.9:p.Leu477Val
ENST00000376970.6:c.4417C>G	ENSP00000366169.3:p.Leu1473Val
ENST00000425460.5:c.4441C>G	ENSP00000407879.1:p.Leu1481Val
ENST00000440075.6:c.346C>G	ENSP00000406273.3:p.Leu116Val
ENST00000595016.1:n.1719C>G
ENST00000596571.5:c.4417C>G	ENSP00000472819.1:p.Leu1473Val
ENST00000598205.5:c.4441C>G	ENSP00000472543.1:p.Leu1481Val
ENST00000601313.5:c.4540C>G	ENSP00000470298.1:p.Leu1514Val
NM_001077186.1:c.4441C>G	NP_001070654.1:p.Leu1481Val
NM_001145809.1:c.4540C>G	NP_001139281.1:p.Leu1514Val
NM_024729.3:c.4417C>G	NP_079005.3:p.Leu1473Val
XM_006723386.2:c.4441C>G	XP_006723449.1:p.Leu1481Val
XM_011527320.1:c.4561C>G	XP_011525622.1:p.Leu1521Val
XM_011527321.1:c.4537C>G	XP_011525623.1:p.Leu1513Val
XM_011527322.1:c.4465C>G	XP_011525624.1:p.Leu1489Val
XM_011527323.1:c.4441C>G	XP_011525625.1:p.Leu1481Val
XM_006723386.4:c.4441C>G	XP_006723449.1:p.Leu1481Val
XM_011527320.2:c.4561C>G	XP_011525622.1:p.Leu1521Val
XM_011527321.2:c.4537C>G	XP_011525623.1:p.Leu1513Val
XM_011527323.2:c.4441C>G	XP_011525625.1:p.Leu1481Val
XM_024451721.1:c.4417C>G	XP_024307489.1:p.Leu1473Val
NM_001077186.2:c.4441C>G	NP_001070654.1:p.Leu1481Val
NM_001145809.2:c.4540C>G MANE Select	NP_001139281.1:p.Leu1514Val
NM_024729.4:c.4417C>G	NP_079005.3:p.Leu1473Val