Canonical Allele Identifier: CA9593782

Gene: MYH14

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50293602G>A , CM000681.2:g.50293602G>A	GRCh38
NC_000019.9:g.50796859G>A , CM000681.1:g.50796859G>A	GRCh37
NC_000019.8:g.55488671G>A	NCBI36
NG_011645.1:g.94975G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001145809.2:c.5384G>A MANE Select	NP_001139281.1:p.Arg1795His
ENST00000642316.2:c.5384G>A MANE Select	ENSP00000493594.1:p.Arg1795His
NM_001077186.1:c.5285G>A	NP_001070654.1:p.Arg1762His
NM_001077186.2:c.5285G>A	NP_001070654.1:p.Arg1762His
NM_001145809.1:c.5384G>A	NP_001139281.1:p.Arg1795His
NM_024729.3:c.5261G>A	NP_079005.3:p.Arg1754His
NM_024729.4:c.5261G>A	NP_079005.3:p.Arg1754His
ENST00000262269.12:c.*745G>A	ENSP00000262269.9:n.*745G>A
ENST00000376970.6:c.5261G>A	ENSP00000366169.3:p.Arg1754His
ENST00000425460.5:c.5285G>A	ENSP00000407879.1:p.Arg1762His
ENST00000425460.6:c.5285G>A	ENSP00000407879.1:p.Arg1762His
ENST00000440075.6:c.1190G>A	ENSP00000406273.3:p.Arg397His
ENST00000595016.1:n.2563G>A
ENST00000596571.5:c.5261G>A	ENSP00000472819.1:p.Arg1754His
ENST00000598205.5:c.5285G>A	ENSP00000472543.1:p.Arg1762His
ENST00000601313.5:c.5384G>A	ENSP00000470298.1:p.Arg1795His
XM_006723386.2:c.5285G>A	XP_006723449.1:p.Arg1762His
XM_006723386.4:c.5285G>A	XP_006723449.1:p.Arg1762His
XM_011527320.1:c.5405G>A	XP_011525622.1:p.Arg1802His
XM_011527320.2:c.5405G>A	XP_011525622.1:p.Arg1802His
XM_011527321.1:c.5381G>A	XP_011525623.1:p.Arg1794His
XM_011527321.2:c.5381G>A	XP_011525623.1:p.Arg1794His
XM_011527322.1:c.5309G>A	XP_011525624.1:p.Arg1770His
XM_011527323.1:c.5285G>A	XP_011525625.1:p.Arg1762His
XM_011527323.2:c.5285G>A	XP_011525625.1:p.Arg1762His
XM_024451721.1:c.5261G>A	XP_024307489.1:p.Arg1754His