Canonical Allele Identifier: CA9593461

Gene: MYH14

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50280312C>T , CM000681.2:g.50280312C>T	GRCh38
NC_000019.9:g.50783569C>T , CM000681.1:g.50783569C>T	GRCh37
NC_000019.8:g.55475381C>T	NCBI36
NG_011645.1:g.81685C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000425460.6:c.4120C>T	ENSP00000407879.1:p.Arg1374Cys
ENST00000642316.2:c.4219C>T MANE Select	ENSP00000493594.1:p.Arg1407Cys
ENST00000262269.12:c.1108C>T	ENSP00000262269.9:p.Arg370Cys
ENST00000376970.6:c.4096C>T	ENSP00000366169.3:p.Arg1366Cys
ENST00000425460.5:c.4120C>T	ENSP00000407879.1:p.Arg1374Cys
ENST00000440075.6:c.25C>T	ENSP00000406273.3:p.Arg9Cys
ENST00000596571.5:c.4096C>T	ENSP00000472819.1:p.Arg1366Cys
ENST00000598205.5:c.4120C>T	ENSP00000472543.1:p.Arg1374Cys
ENST00000601313.5:c.4219C>T	ENSP00000470298.1:p.Arg1407Cys
NM_001077186.1:c.4120C>T	NP_001070654.1:p.Arg1374Cys
NM_001145809.1:c.4219C>T	NP_001139281.1:p.Arg1407Cys
NM_024729.3:c.4096C>T	NP_079005.3:p.Arg1366Cys
XM_006723386.2:c.4120C>T	XP_006723449.1:p.Arg1374Cys
XM_011527320.1:c.4240C>T	XP_011525622.1:p.Arg1414Cys
XM_011527321.1:c.4216C>T	XP_011525623.1:p.Arg1406Cys
XM_011527322.1:c.4144C>T	XP_011525624.1:p.Arg1382Cys
XM_011527323.1:c.4120C>T	XP_011525625.1:p.Arg1374Cys
XM_006723386.4:c.4120C>T	XP_006723449.1:p.Arg1374Cys
XM_011527320.2:c.4240C>T	XP_011525622.1:p.Arg1414Cys
XM_011527321.2:c.4216C>T	XP_011525623.1:p.Arg1406Cys
XM_011527323.2:c.4120C>T	XP_011525625.1:p.Arg1374Cys
XM_024451721.1:c.4096C>T	XP_024307489.1:p.Arg1366Cys
NM_001077186.2:c.4120C>T	NP_001070654.1:p.Arg1374Cys
NM_001145809.2:c.4219C>T MANE Select	NP_001139281.1:p.Arg1407Cys
NM_024729.4:c.4096C>T	NP_079005.3:p.Arg1366Cys