Canonical Allele Identifier: CA1152147785

Gene: PARK7

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.7985095A= , CM000663.2:g.7985095A=	GRCh38
NC_000001.10:g.8045155A= , CM000663.1:g.8045155A=	GRCh37
NC_000001.9:g.7967742A=	NCBI36
NG_008271.1:g.28442A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338639.10:c.*41A= MANE Select	ENSP00000340278.5:n.*41A=
ENST00000338639.9:c.*41A=	ENSP00000340278.5:n.*41A=
ENST00000377488.5:c.*41A=	ENSP00000366708.1:n.*41A=
ENST00000377491.5:c.*41A=	ENSP00000366711.1:n.*41A=
ENST00000377493.9:c.*41A=	ENSP00000466242.1:n.*41A=
ENST00000469225.1:c.524A=	ENSP00000466756.1:n.524A=
ENST00000493678.5:c.*41A=	ENSP00000418770.1:n.*41A=
NM_001123377.1:c.*41A=	NP_001116849.1:n.*41A=
NM_007262.4:c.*41A=	NP_009193.2:n.*41A=
XM_005263424.2:c.*41A=	XP_005263481.1:n.*41A=
XM_005263424.3:c.*41A=	XP_005263481.1:n.*41A=
NM_007262.5:c.*41A= MANE Select	NP_009193.2:n.*41A=
NM_001123377.2:c.*41A=	NP_001116849.1:n.*41A=