Canonical Allele Identifier: CA406958765

Gene: MYH14

Linked Data

• MyVariant Identifiers: chr19:g.50789740T>G (hg19) ; chr19:g.50286483T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50286483T>G , CM000681.2:g.50286483T>G	GRCh38
NC_000019.9:g.50789740T>G , CM000681.1:g.50789740T>G	GRCh37
NC_000019.8:g.55481552T>G	NCBI36
NG_011645.1:g.87856T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000425460.6:c.4442T>G	ENSP00000407879.1:p.Leu1481Arg
ENST00000642316.2:c.4541T>G MANE Select	ENSP00000493594.1:p.Leu1514Arg
ENST00000262269.12:c.1430T>G	ENSP00000262269.9:p.Leu477Arg
ENST00000376970.6:c.4418T>G	ENSP00000366169.3:p.Leu1473Arg
ENST00000425460.5:c.4442T>G	ENSP00000407879.1:p.Leu1481Arg
ENST00000440075.6:c.347T>G	ENSP00000406273.3:p.Leu116Arg
ENST00000595016.1:n.1720T>G
ENST00000596571.5:c.4418T>G	ENSP00000472819.1:p.Leu1473Arg
ENST00000598205.5:c.4442T>G	ENSP00000472543.1:p.Leu1481Arg
ENST00000601313.5:c.4541T>G	ENSP00000470298.1:p.Leu1514Arg
NM_001077186.1:c.4442T>G	NP_001070654.1:p.Leu1481Arg
NM_001145809.1:c.4541T>G	NP_001139281.1:p.Leu1514Arg
NM_024729.3:c.4418T>G	NP_079005.3:p.Leu1473Arg
XM_006723386.2:c.4442T>G	XP_006723449.1:p.Leu1481Arg
XM_011527320.1:c.4562T>G	XP_011525622.1:p.Leu1521Arg
XM_011527321.1:c.4538T>G	XP_011525623.1:p.Leu1513Arg
XM_011527322.1:c.4466T>G	XP_011525624.1:p.Leu1489Arg
XM_011527323.1:c.4442T>G	XP_011525625.1:p.Leu1481Arg
XM_006723386.4:c.4442T>G	XP_006723449.1:p.Leu1481Arg
XM_011527320.2:c.4562T>G	XP_011525622.1:p.Leu1521Arg
XM_011527321.2:c.4538T>G	XP_011525623.1:p.Leu1513Arg
XM_011527323.2:c.4442T>G	XP_011525625.1:p.Leu1481Arg
XM_024451721.1:c.4418T>G	XP_024307489.1:p.Leu1473Arg
NM_001077186.2:c.4442T>G	NP_001070654.1:p.Leu1481Arg
NM_001145809.2:c.4541T>G MANE Select	NP_001139281.1:p.Leu1514Arg
NM_024729.4:c.4418T>G	NP_079005.3:p.Leu1473Arg