Canonical Allele Identifier: CA406958792

Gene: MYH14

Linked Data

• dbSNP Id: rs1340339207
• gnomAD v2: 19-50789753-G-C
• MyVariant Identifiers: chr19:g.50789753G>C (hg19) ; chr19:g.50286496G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50286496G>C , CM000681.2:g.50286496G>C	GRCh38
NC_000019.9:g.50789753G>C , CM000681.1:g.50789753G>C	GRCh37
NC_000019.8:g.55481565G>C	NCBI36
NG_011645.1:g.87869G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000425460.6:c.4455G>C	ENSP00000407879.1:p.Glu1485Asp
ENST00000642316.2:c.4554G>C MANE Select	ENSP00000493594.1:p.Glu1518Asp
ENST00000262269.12:c.1443G>C	ENSP00000262269.9:p.Glu481Asp
ENST00000376970.6:c.4431G>C	ENSP00000366169.3:p.Glu1477Asp
ENST00000425460.5:c.4455G>C	ENSP00000407879.1:p.Glu1485Asp
ENST00000440075.6:c.360G>C	ENSP00000406273.3:p.Glu120Asp
ENST00000595016.1:n.1733G>C
ENST00000596571.5:c.4431G>C	ENSP00000472819.1:p.Glu1477Asp
ENST00000598205.5:c.4455G>C	ENSP00000472543.1:p.Glu1485Asp
ENST00000601313.5:c.4554G>C	ENSP00000470298.1:p.Glu1518Asp
NM_001077186.1:c.4455G>C	NP_001070654.1:p.Glu1485Asp
NM_001145809.1:c.4554G>C	NP_001139281.1:p.Glu1518Asp
NM_024729.3:c.4431G>C	NP_079005.3:p.Glu1477Asp
XM_006723386.2:c.4455G>C	XP_006723449.1:p.Glu1485Asp
XM_011527320.1:c.4575G>C	XP_011525622.1:p.Glu1525Asp
XM_011527321.1:c.4551G>C	XP_011525623.1:p.Glu1517Asp
XM_011527322.1:c.4479G>C	XP_011525624.1:p.Glu1493Asp
XM_011527323.1:c.4455G>C	XP_011525625.1:p.Glu1485Asp
XM_006723386.4:c.4455G>C	XP_006723449.1:p.Glu1485Asp
XM_011527320.2:c.4575G>C	XP_011525622.1:p.Glu1525Asp
XM_011527321.2:c.4551G>C	XP_011525623.1:p.Glu1517Asp
XM_011527323.2:c.4455G>C	XP_011525625.1:p.Glu1485Asp
XM_024451721.1:c.4431G>C	XP_024307489.1:p.Glu1477Asp
NM_001077186.2:c.4455G>C	NP_001070654.1:p.Glu1485Asp
NM_001145809.2:c.4554G>C MANE Select	NP_001139281.1:p.Glu1518Asp
NM_024729.4:c.4431G>C	NP_079005.3:p.Glu1477Asp