Canonical Allele Identifier: CA1139775651

Gene: PARK7

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.7982766G= , CM000663.2:g.7982766G=	GRCh38
NC_000001.10:g.8042826G= , CM000663.1:g.8042826G=	GRCh37
NC_000001.9:g.7965413G=	NCBI36
NG_008271.1:g.26113G=

Transcript Alleles

HGVS	Amino-acid Change
NM_007262.5:c.410-2128G= MANE Select	NP_009193.2:n.410-2128G=
ENST00000338639.10:c.410-2128G= MANE Select	ENSP00000340278.5:n.410-2128G=
NM_001123377.1:c.410-2128G=	NP_001116849.1:n.410-2128G=
NM_001123377.2:c.410-2128G=	NP_001116849.1:n.410-2128G=
NM_007262.4:c.410-2128G=	NP_009193.2:n.410-2128G=
ENST00000338639.9:c.410-2128G=	ENSP00000340278.5:n.410-2128G=
ENST00000377488.5:c.410-2128G=	ENSP00000366708.1:n.410-2128G=
ENST00000377491.5:c.410-2128G=	ENSP00000366711.1:n.410-2128G=
ENST00000377493.9:c.350-2128G=	ENSP00000466242.1:n.350-2128G=
ENST00000469225.1:c.293-2098G=	ENSP00000466756.1:n.293-2098G=
ENST00000493373.5:c.410-2128G=	ENSP00000465404.1:n.410-2128G=
ENST00000493678.5:c.410-2128G=	ENSP00000418770.1:n.410-2128G=
XM_005263424.2:c.410-2128G=	XP_005263481.1:n.410-2128G=
XM_005263424.3:c.410-2128G=	XP_005263481.1:n.410-2128G=