Canonical Allele Identifier: CA406949008

Gene: MYH14

Linked Data

• gnomAD v4: 19-50268349-G-T
• MyVariant Identifiers: chr19:g.50771606G>T (hg19) ; chr19:g.50268349G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50268349G>T , CM000681.2:g.50268349G>T	GRCh38
NC_000019.9:g.50771606G>T , CM000681.1:g.50771606G>T	GRCh37
NC_000019.8:g.55463418G>T	NCBI36
NG_011645.1:g.69722G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000425460.6:c.2916G>T	ENSP00000407879.1:p.Arg972Ser
ENST00000642316.2:c.3015G>T MANE Select	ENSP00000493594.1:p.Arg1005Ser
ENST00000262269.12:c.-97G>T	ENSP00000262269.9:n.-97G>T
ENST00000376970.6:c.2892G>T	ENSP00000366169.3:p.Arg964Ser
ENST00000425460.5:c.2916G>T	ENSP00000407879.1:p.Arg972Ser
ENST00000440075.6:c.-727-7642G>T	ENSP00000406273.3:n.-727-7642G>T
ENST00000596571.5:c.2892G>T	ENSP00000472819.1:p.Arg964Ser
ENST00000598205.5:c.2916G>T	ENSP00000472543.1:p.Arg972Ser
ENST00000599920.5:c.2916G>T	ENSP00000469573.1:p.Arg972Ser
ENST00000601313.5:c.3015G>T	ENSP00000470298.1:p.Arg1005Ser
NM_001077186.1:c.2916G>T	NP_001070654.1:p.Arg972Ser
NM_001145809.1:c.3015G>T	NP_001139281.1:p.Arg1005Ser
NM_024729.3:c.2892G>T	NP_079005.3:p.Arg964Ser
XM_006723386.2:c.2916G>T	XP_006723449.1:p.Arg972Ser
XM_011527320.1:c.3036G>T	XP_011525622.1:p.Arg1012Ser
XM_011527321.1:c.3012G>T	XP_011525623.1:p.Arg1004Ser
XM_011527322.1:c.2940G>T	XP_011525624.1:p.Arg980Ser
XM_011527323.1:c.2916G>T	XP_011525625.1:p.Arg972Ser
XM_006723386.4:c.2916G>T	XP_006723449.1:p.Arg972Ser
XM_011527320.2:c.3036G>T	XP_011525622.1:p.Arg1012Ser
XM_011527321.2:c.3012G>T	XP_011525623.1:p.Arg1004Ser
XM_011527323.2:c.2916G>T	XP_011525625.1:p.Arg972Ser
XM_024451721.1:c.2892G>T	XP_024307489.1:p.Arg964Ser
NM_001077186.2:c.2916G>T	NP_001070654.1:p.Arg972Ser
NM_001145809.2:c.3015G>T MANE Select	NP_001139281.1:p.Arg1005Ser
NM_024729.4:c.2892G>T	NP_079005.3:p.Arg964Ser