Canonical Allele Identifier: CA2838206026
Gene: MYH14 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50268349del , CM000681.2:g.50268349del GRCh38
NC_000019.9:g.50771606del , CM000681.1:g.50771606del GRCh37
NC_000019.8:g.55463418del NCBI36
NG_011645.1:g.69722del

Transcript Alleles

HGVS Amino-acid Change
ENST00000425460.6:c.2916del ENSP00000407879.1:p.Arg972SerfsTer9
ENST00000642316.2:c.3015del MANE Select ENSP00000493594.1:p.Arg1005SerfsTer9
ENST00000262269.12:c.-97del ENSP00000262269.9:n.-97del
ENST00000376970.6:c.2892del ENSP00000366169.3:p.Arg964SerfsTer9
ENST00000425460.5:c.2916del ENSP00000407879.1:p.Arg972SerfsTer9
ENST00000440075.6:c.-727-7642del ENSP00000406273.3:n.-727-7642del
ENST00000596571.5:c.2892del ENSP00000472819.1:p.Arg964SerfsTer9
ENST00000598205.5:c.2916del ENSP00000472543.1:p.Arg972SerfsTer9
ENST00000599920.5:c.2916del ENSP00000469573.1:p.Arg972SerfsTer9
ENST00000601313.5:c.3015del ENSP00000470298.1:p.Arg1005SerfsTer9
NM_001077186.1:c.2916del NP_001070654.1:p.Arg972SerfsTer9
NM_001145809.1:c.3015del NP_001139281.1:p.Arg1005SerfsTer9
NM_024729.3:c.2892del NP_079005.3:p.Arg964SerfsTer9
XM_006723386.2:c.2916del XP_006723449.1:p.Arg972SerfsTer9
XM_011527320.1:c.3036del XP_011525622.1:p.Arg1012SerfsTer9
XM_011527321.1:c.3012del XP_011525623.1:p.Arg1004SerfsTer9
XM_011527322.1:c.2940del XP_011525624.1:p.Arg980SerfsTer9
XM_011527323.1:c.2916del XP_011525625.1:p.Arg972SerfsTer9
XM_006723386.4:c.2916del XP_006723449.1:p.Arg972SerfsTer9
XM_011527320.2:c.3036del XP_011525622.1:p.Arg1012SerfsTer9
XM_011527321.2:c.3012del XP_011525623.1:p.Arg1004SerfsTer9
XM_011527323.2:c.2916del XP_011525625.1:p.Arg972SerfsTer9
XM_024451721.1:c.2892del XP_024307489.1:p.Arg964SerfsTer9
NM_001077186.2:c.2916del NP_001070654.1:p.Arg972SerfsTer9
NM_001145809.2:c.3015del MANE Select NP_001139281.1:p.Arg1005SerfsTer9
NM_024729.4:c.2892del NP_079005.3:p.Arg964SerfsTer9