Canonical Allele Identifier: CA508177931

Gene: MYH14

Linked Data

• MyVariant Identifiers: chr19:g.50789747A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50286490A>C , CM000681.2:g.50286490A>C	GRCh38
NC_000019.9:g.50789747A>C , CM000681.1:g.50789747A>C	GRCh37
NC_000019.8:g.55481559A>C	NCBI36
NG_011645.1:g.87863A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000425460.6:c.4449A>C	ENSP00000407879.1:p.Ala1483=
ENST00000642316.2:c.4548A>C MANE Select	ENSP00000493594.1:p.Ala1516=
ENST00000262269.12:c.1437A>C	ENSP00000262269.9:p.Ala479=
ENST00000376970.6:c.4425A>C	ENSP00000366169.3:p.Ala1475=
ENST00000425460.5:c.4449A>C	ENSP00000407879.1:p.Ala1483=
ENST00000440075.6:c.354A>C	ENSP00000406273.3:p.Ala118=
ENST00000595016.1:n.1727A>C
ENST00000596571.5:c.4425A>C	ENSP00000472819.1:p.Ala1475=
ENST00000598205.5:c.4449A>C	ENSP00000472543.1:p.Ala1483=
ENST00000601313.5:c.4548A>C	ENSP00000470298.1:p.Ala1516=
NM_001077186.1:c.4449A>C	NP_001070654.1:p.Ala1483=
NM_001145809.1:c.4548A>C	NP_001139281.1:p.Ala1516=
NM_024729.3:c.4425A>C	NP_079005.3:p.Ala1475=
XM_006723386.2:c.4449A>C	XP_006723449.1:p.Ala1483=
XM_011527320.1:c.4569A>C	XP_011525622.1:p.Ala1523=
XM_011527321.1:c.4545A>C	XP_011525623.1:p.Ala1515=
XM_011527322.1:c.4473A>C	XP_011525624.1:p.Ala1491=
XM_011527323.1:c.4449A>C	XP_011525625.1:p.Ala1483=
XM_006723386.4:c.4449A>C	XP_006723449.1:p.Ala1483=
XM_011527320.2:c.4569A>C	XP_011525622.1:p.Ala1523=
XM_011527321.2:c.4545A>C	XP_011525623.1:p.Ala1515=
XM_011527323.2:c.4449A>C	XP_011525625.1:p.Ala1483=
XM_024451721.1:c.4425A>C	XP_024307489.1:p.Ala1475=
NM_001077186.2:c.4449A>C	NP_001070654.1:p.Ala1483=
NM_001145809.2:c.4548A>C MANE Select	NP_001139281.1:p.Ala1516=
NM_024729.4:c.4425A>C	NP_079005.3:p.Ala1475=