Canonical Allele Identifier: CA9593082

Gene: MYH14

Linked Data

• dbSNP Id: rs747892579
• ExAC: 19:50771581 G / A
• gnomAD v2: 19-50771581-G-A
• gnomAD v3: 19-50268324-G-A
• gnomAD v4: 19-50268324-G-A
• COSMIC: COSM999623 ; COSM999624
• MyVariant Identifiers: chr19:g.50771581G>A (hg19) ; chr19:g.50268324G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50268324G>A , CM000681.2:g.50268324G>A	GRCh38
NC_000019.9:g.50771581G>A , CM000681.1:g.50771581G>A	GRCh37
NC_000019.8:g.55463393G>A	NCBI36
NG_011645.1:g.69697G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000425460.6:c.2891G>A	ENSP00000407879.1:p.Arg964His
ENST00000642316.2:c.2990G>A MANE Select	ENSP00000493594.1:p.Arg997His
ENST00000376970.6:c.2867G>A	ENSP00000366169.3:p.Arg956His
ENST00000425460.5:c.2891G>A	ENSP00000407879.1:p.Arg964His
ENST00000440075.6:c.-727-7667G>A	ENSP00000406273.3:n.-727-7667G>A
ENST00000596571.5:c.2867G>A	ENSP00000472819.1:p.Arg956His
ENST00000598205.5:c.2891G>A	ENSP00000472543.1:p.Arg964His
ENST00000599920.5:c.2891G>A	ENSP00000469573.1:p.Arg964His
ENST00000601313.5:c.2990G>A	ENSP00000470298.1:p.Arg997His
NM_001077186.1:c.2891G>A	NP_001070654.1:p.Arg964His
NM_001145809.1:c.2990G>A	NP_001139281.1:p.Arg997His
NM_024729.3:c.2867G>A	NP_079005.3:p.Arg956His
XM_006723386.2:c.2891G>A	XP_006723449.1:p.Arg964His
XM_011527320.1:c.3011G>A	XP_011525622.1:p.Arg1004His
XM_011527321.1:c.2987G>A	XP_011525623.1:p.Arg996His
XM_011527322.1:c.2915G>A	XP_011525624.1:p.Arg972His
XM_011527323.1:c.2891G>A	XP_011525625.1:p.Arg964His
XM_006723386.4:c.2891G>A	XP_006723449.1:p.Arg964His
XM_011527320.2:c.3011G>A	XP_011525622.1:p.Arg1004His
XM_011527321.2:c.2987G>A	XP_011525623.1:p.Arg996His
XM_011527323.2:c.2891G>A	XP_011525625.1:p.Arg964His
XM_024451721.1:c.2867G>A	XP_024307489.1:p.Arg956His
NM_001077186.2:c.2891G>A	NP_001070654.1:p.Arg964His
NM_001145809.2:c.2990G>A MANE Select	NP_001139281.1:p.Arg997His
NM_024729.4:c.2867G>A	NP_079005.3:p.Arg956His