Canonical Allele Identifier: CA406949039

Gene: MYH14

Linked Data

• gnomAD v4: 19-50268355-G-C
• MyVariant Identifiers: chr19:g.50771612G>C (hg19) ; chr19:g.50268355G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50268355G>C , CM000681.2:g.50268355G>C	GRCh38
NC_000019.9:g.50771612G>C , CM000681.1:g.50771612G>C	GRCh37
NC_000019.8:g.55463424G>C	NCBI36
NG_011645.1:g.69728G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000425460.6:c.2922G>C	ENSP00000407879.1:p.Gln974His
ENST00000642316.2:c.3021G>C MANE Select	ENSP00000493594.1:p.Gln1007His
ENST00000262269.12:c.-91G>C	ENSP00000262269.9:n.-91G>C
ENST00000376970.6:c.2898G>C	ENSP00000366169.3:p.Gln966His
ENST00000425460.5:c.2922G>C	ENSP00000407879.1:p.Gln974His
ENST00000440075.6:c.-727-7636G>C	ENSP00000406273.3:n.-727-7636G>C
ENST00000596571.5:c.2898G>C	ENSP00000472819.1:p.Gln966His
ENST00000598205.5:c.2922G>C	ENSP00000472543.1:p.Gln974His
ENST00000599920.5:c.2922G>C	ENSP00000469573.1:p.Gln974His
ENST00000601313.5:c.3021G>C	ENSP00000470298.1:p.Gln1007His
NM_001077186.1:c.2922G>C	NP_001070654.1:p.Gln974His
NM_001145809.1:c.3021G>C	NP_001139281.1:p.Gln1007His
NM_024729.3:c.2898G>C	NP_079005.3:p.Gln966His
XM_006723386.2:c.2922G>C	XP_006723449.1:p.Gln974His
XM_011527320.1:c.3042G>C	XP_011525622.1:p.Gln1014His
XM_011527321.1:c.3018G>C	XP_011525623.1:p.Gln1006His
XM_011527322.1:c.2946G>C	XP_011525624.1:p.Gln982His
XM_011527323.1:c.2922G>C	XP_011525625.1:p.Gln974His
XM_006723386.4:c.2922G>C	XP_006723449.1:p.Gln974His
XM_011527320.2:c.3042G>C	XP_011525622.1:p.Gln1014His
XM_011527321.2:c.3018G>C	XP_011525623.1:p.Gln1006His
XM_011527323.2:c.2922G>C	XP_011525625.1:p.Gln974His
XM_024451721.1:c.2898G>C	XP_024307489.1:p.Gln966His
NM_001077186.2:c.2922G>C	NP_001070654.1:p.Gln974His
NM_001145809.2:c.3021G>C MANE Select	NP_001139281.1:p.Gln1007His
NM_024729.4:c.2898G>C	NP_079005.3:p.Gln966His