Canonical Allele Identifier: CA9593077

Gene: MYH14

Linked Data

• ClinVar Variation Id: 1805908
• ClinVar RCV Id: RCV002470192
• dbSNP Id: rs758910308
• ExAC: 19:50771520 G / C
• gnomAD v2: 19-50771520-G-C
• gnomAD v4: 19-50268263-G-C
• MyVariant Identifiers: chr19:g.50771520G>C (hg19) ; chr19:g.50268263G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50268263G>C , CM000681.2:g.50268263G>C	GRCh38
NC_000019.9:g.50771520G>C , CM000681.1:g.50771520G>C	GRCh37
NC_000019.8:g.55463332G>C	NCBI36
NG_011645.1:g.69636G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000425460.6:c.2830G>C	ENSP00000407879.1:p.Glu944Gln
ENST00000642316.2:c.2929G>C MANE Select	ENSP00000493594.1:p.Glu977Gln
ENST00000376970.6:c.2806G>C	ENSP00000366169.3:p.Glu936Gln
ENST00000425460.5:c.2830G>C	ENSP00000407879.1:p.Glu944Gln
ENST00000440075.6:c.-727-7728G>C	ENSP00000406273.3:n.-727-7728G>C
ENST00000596571.5:c.2806G>C	ENSP00000472819.1:p.Glu936Gln
ENST00000598205.5:c.2830G>C	ENSP00000472543.1:p.Glu944Gln
ENST00000599920.5:c.2830G>C	ENSP00000469573.1:p.Glu944Gln
ENST00000601313.5:c.2929G>C	ENSP00000470298.1:p.Glu977Gln
NM_001077186.1:c.2830G>C	NP_001070654.1:p.Glu944Gln
NM_001145809.1:c.2929G>C	NP_001139281.1:p.Glu977Gln
NM_024729.3:c.2806G>C	NP_079005.3:p.Glu936Gln
XM_006723386.2:c.2830G>C	XP_006723449.1:p.Glu944Gln
XM_011527320.1:c.2950G>C	XP_011525622.1:p.Glu984Gln
XM_011527321.1:c.2926G>C	XP_011525623.1:p.Glu976Gln
XM_011527322.1:c.2854G>C	XP_011525624.1:p.Glu952Gln
XM_011527323.1:c.2830G>C	XP_011525625.1:p.Glu944Gln
XM_006723386.4:c.2830G>C	XP_006723449.1:p.Glu944Gln
XM_011527320.2:c.2950G>C	XP_011525622.1:p.Glu984Gln
XM_011527321.2:c.2926G>C	XP_011525623.1:p.Glu976Gln
XM_011527323.2:c.2830G>C	XP_011525625.1:p.Glu944Gln
XM_024451721.1:c.2806G>C	XP_024307489.1:p.Glu936Gln
NM_001077186.2:c.2830G>C	NP_001070654.1:p.Glu944Gln
NM_001145809.2:c.2929G>C MANE Select	NP_001139281.1:p.Glu977Gln
NM_024729.4:c.2806G>C	NP_079005.3:p.Glu936Gln