Canonical Allele Identifier: CA2340825494

Gene: MYH14

Linked Data

• dbSNP Id: rs2035891403

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50286494_50286496del , CM000681.2:g.50286494_50286496del	GRCh38
NC_000019.9:g.50789751_50789753del , CM000681.1:g.50789751_50789753del	GRCh37
NC_000019.8:g.55481563_55481565del	NCBI36
NG_011645.1:g.87867_87869del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000425460.6:c.4453_4455del	ENSP00000407879.1:p.Glu1485del
ENST00000642316.2:c.4552_4554del MANE Select	ENSP00000493594.1:p.Glu1518del
ENST00000262269.12:c.1441_1443del	ENSP00000262269.9:p.Glu481del
ENST00000376970.6:c.4429_4431del	ENSP00000366169.3:p.Glu1477del
ENST00000425460.5:c.4453_4455del	ENSP00000407879.1:p.Glu1485del
ENST00000440075.6:c.358_360del	ENSP00000406273.3:p.Glu120del
ENST00000595016.1:n.1731_1733del
ENST00000596571.5:c.4429_4431del	ENSP00000472819.1:p.Glu1477del
ENST00000598205.5:c.4453_4455del	ENSP00000472543.1:p.Glu1485del
ENST00000601313.5:c.4552_4554del	ENSP00000470298.1:p.Glu1518del
NM_001077186.1:c.4453_4455del	NP_001070654.1:p.Glu1485del
NM_001145809.1:c.4552_4554del	NP_001139281.1:p.Glu1518del
NM_024729.3:c.4429_4431del	NP_079005.3:p.Glu1477del
XM_006723386.2:c.4453_4455del	XP_006723449.1:p.Glu1485del
XM_011527320.1:c.4573_4575del	XP_011525622.1:p.Glu1525del
XM_011527321.1:c.4549_4551del	XP_011525623.1:p.Glu1517del
XM_011527322.1:c.4477_4479del	XP_011525624.1:p.Glu1493del
XM_011527323.1:c.4453_4455del	XP_011525625.1:p.Glu1485del
XM_006723386.4:c.4453_4455del	XP_006723449.1:p.Glu1485del
XM_011527320.2:c.4573_4575del	XP_011525622.1:p.Glu1525del
XM_011527321.2:c.4549_4551del	XP_011525623.1:p.Glu1517del
XM_011527323.2:c.4453_4455del	XP_011525625.1:p.Glu1485del
XM_024451721.1:c.4429_4431del	XP_024307489.1:p.Glu1477del
NM_001077186.2:c.4453_4455del	NP_001070654.1:p.Glu1485del
NM_001145809.2:c.4552_4554del MANE Select	NP_001139281.1:p.Glu1518del
NM_024729.4:c.4429_4431del	NP_079005.3:p.Glu1477del