Canonical Allele Identifier: CA9593085
Gene: MYH14 HGNC NCBI

Linked Data

dbSNP Id: rs771027433

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50268355G>A , CM000681.2:g.50268355G>A GRCh38
NC_000019.9:g.50771612G>A , CM000681.1:g.50771612G>A GRCh37
NC_000019.8:g.55463424G>A NCBI36
NG_011645.1:g.69728G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000425460.6:c.2922G>A ENSP00000407879.1:p.Gln974=
ENST00000642316.2:c.3021G>A MANE Select ENSP00000493594.1:p.Gln1007=
ENST00000262269.12:c.-91G>A ENSP00000262269.9:n.-91G>A
ENST00000376970.6:c.2898G>A ENSP00000366169.3:p.Gln966=
ENST00000425460.5:c.2922G>A ENSP00000407879.1:p.Gln974=
ENST00000440075.6:c.-727-7636G>A ENSP00000406273.3:n.-727-7636G>A
ENST00000596571.5:c.2898G>A ENSP00000472819.1:p.Gln966=
ENST00000598205.5:c.2922G>A ENSP00000472543.1:p.Gln974=
ENST00000599920.5:c.2922G>A ENSP00000469573.1:p.Gln974=
ENST00000601313.5:c.3021G>A ENSP00000470298.1:p.Gln1007=
NM_001077186.1:c.2922G>A NP_001070654.1:p.Gln974=
NM_001145809.1:c.3021G>A NP_001139281.1:p.Gln1007=
NM_024729.3:c.2898G>A NP_079005.3:p.Gln966=
XM_006723386.2:c.2922G>A XP_006723449.1:p.Gln974=
XM_011527320.1:c.3042G>A XP_011525622.1:p.Gln1014=
XM_011527321.1:c.3018G>A XP_011525623.1:p.Gln1006=
XM_011527322.1:c.2946G>A XP_011525624.1:p.Gln982=
XM_011527323.1:c.2922G>A XP_011525625.1:p.Gln974=
XM_006723386.4:c.2922G>A XP_006723449.1:p.Gln974=
XM_011527320.2:c.3042G>A XP_011525622.1:p.Gln1014=
XM_011527321.2:c.3018G>A XP_011525623.1:p.Gln1006=
XM_011527323.2:c.2922G>A XP_011525625.1:p.Gln974=
XM_024451721.1:c.2898G>A XP_024307489.1:p.Gln966=
NM_001077186.2:c.2922G>A NP_001070654.1:p.Gln974=
NM_001145809.2:c.3021G>A MANE Select NP_001139281.1:p.Gln1007=
NM_024729.4:c.2898G>A NP_079005.3:p.Gln966=