Canonical Allele Identifier: CA406949002

Gene: MYH14

Linked Data

• MyVariant Identifiers: chr19:g.50771605G>C (hg19) ; chr19:g.50268348G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50268348G>C , CM000681.2:g.50268348G>C	GRCh38
NC_000019.9:g.50771605G>C , CM000681.1:g.50771605G>C	GRCh37
NC_000019.8:g.55463417G>C	NCBI36
NG_011645.1:g.69721G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000425460.6:c.2915G>C	ENSP00000407879.1:p.Arg972Thr
ENST00000642316.2:c.3014G>C MANE Select	ENSP00000493594.1:p.Arg1005Thr
ENST00000262269.12:c.-98G>C	ENSP00000262269.9:n.-98G>C
ENST00000376970.6:c.2891G>C	ENSP00000366169.3:p.Arg964Thr
ENST00000425460.5:c.2915G>C	ENSP00000407879.1:p.Arg972Thr
ENST00000440075.6:c.-727-7643G>C	ENSP00000406273.3:n.-727-7643G>C
ENST00000596571.5:c.2891G>C	ENSP00000472819.1:p.Arg964Thr
ENST00000598205.5:c.2915G>C	ENSP00000472543.1:p.Arg972Thr
ENST00000599920.5:c.2915G>C	ENSP00000469573.1:p.Arg972Thr
ENST00000601313.5:c.3014G>C	ENSP00000470298.1:p.Arg1005Thr
NM_001077186.1:c.2915G>C	NP_001070654.1:p.Arg972Thr
NM_001145809.1:c.3014G>C	NP_001139281.1:p.Arg1005Thr
NM_024729.3:c.2891G>C	NP_079005.3:p.Arg964Thr
XM_006723386.2:c.2915G>C	XP_006723449.1:p.Arg972Thr
XM_011527320.1:c.3035G>C	XP_011525622.1:p.Arg1012Thr
XM_011527321.1:c.3011G>C	XP_011525623.1:p.Arg1004Thr
XM_011527322.1:c.2939G>C	XP_011525624.1:p.Arg980Thr
XM_011527323.1:c.2915G>C	XP_011525625.1:p.Arg972Thr
XM_006723386.4:c.2915G>C	XP_006723449.1:p.Arg972Thr
XM_011527320.2:c.3035G>C	XP_011525622.1:p.Arg1012Thr
XM_011527321.2:c.3011G>C	XP_011525623.1:p.Arg1004Thr
XM_011527323.2:c.2915G>C	XP_011525625.1:p.Arg972Thr
XM_024451721.1:c.2891G>C	XP_024307489.1:p.Arg964Thr
NM_001077186.2:c.2915G>C	NP_001070654.1:p.Arg972Thr
NM_001145809.2:c.3014G>C MANE Select	NP_001139281.1:p.Arg1005Thr
NM_024729.4:c.2891G>C	NP_079005.3:p.Arg964Thr