Canonical Allele Identifier: CA1140886314

Gene: PARK7

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.7962863G= , CM000663.2:g.7962863G=	GRCh38
NC_000001.10:g.8022923G= , CM000663.1:g.8022923G=	GRCh37
NC_000001.9:g.7945510G=	NCBI36
NG_008271.1:g.6210G=

Transcript Alleles

HGVS	Amino-acid Change
NM_007262.5:c.78G= MANE Select	NP_009193.2:p.Met26=
ENST00000338639.10:c.78G= MANE Select	ENSP00000340278.5:p.Met26=
NM_001123377.1:c.78G=	NP_001116849.1:p.Met26=
NM_001123377.2:c.78G=	NP_001116849.1:p.Met26=
NM_007262.4:c.78G=	NP_009193.2:p.Met26=
ENST00000338639.9:c.78G=	ENSP00000340278.5:p.Met26=
ENST00000377488.5:c.78G=	ENSP00000366708.1:p.Met26=
ENST00000377491.5:c.78G=	ENSP00000366711.1:p.Met26=
ENST00000377493.9:c.78G=	ENSP00000466242.1:p.Met26=
ENST00000460192.5:n.174G=
ENST00000465354.5:n.147G=
ENST00000493373.5:c.78G=	ENSP00000465404.1:p.Met26=
ENST00000493678.5:c.78G=	ENSP00000418770.1:p.Met26=
ENST00000497113.1:n.97G=
XM_005263424.2:c.78G=	XP_005263481.1:p.Met26=
XM_005263424.3:c.78G=	XP_005263481.1:p.Met26=