Canonical Allele Identifier: CA415839079

Gene: PARK7

Linked Data

• MyVariant Identifiers: chr1:g.8045012G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.7984952G>A , CM000663.2:g.7984952G>A	GRCh38
NC_000001.10:g.8045012G>A , CM000663.1:g.8045012G>A	GRCh37
NC_000001.9:g.7967599G>A	NCBI36
NG_008271.1:g.28299G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338639.10:c.468G>A MANE Select	ENSP00000340278.5:p.Arg156=
ENST00000338639.9:c.468G>A	ENSP00000340278.5:p.Arg156=
ENST00000377488.5:c.468G>A	ENSP00000366708.1:p.Arg156=
ENST00000377491.5:c.468G>A	ENSP00000366711.1:p.Arg156=
ENST00000377493.9:c.408G>A	ENSP00000466242.1:p.Arg136=
ENST00000469225.1:c.381G>A	ENSP00000466756.1:p.Arg127=
ENST00000493373.5:c.468G>A	ENSP00000465404.1:p.Arg156=
ENST00000493678.5:c.468G>A	ENSP00000418770.1:p.Arg156=
NM_001123377.1:c.468G>A	NP_001116849.1:p.Arg156=
NM_007262.4:c.468G>A	NP_009193.2:p.Arg156=
XM_005263424.2:c.468G>A	XP_005263481.1:p.Arg156=
XM_005263424.3:c.468G>A	XP_005263481.1:p.Arg156=
NM_007262.5:c.468G>A MANE Select	NP_009193.2:p.Arg156=
NM_001123377.2:c.468G>A	NP_001116849.1:p.Arg156=