Canonical Allele Identifier: CA1152179211

Gene: PARK7

Linked Data

• dbSNP Id: rs1282351669

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.7965253T>C , CM000663.2:g.7965253T>C	GRCh38
NC_000001.10:g.8025313T>C , CM000663.1:g.8025313T>C	GRCh37
NC_000001.9:g.7947900T>C	NCBI36
NG_008271.1:g.8600T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000338639.10:c.91-71T>C MANE Select	ENSP00000340278.5:n.91-71T>C
ENST00000338639.9:c.91-71T>C	ENSP00000340278.5:n.91-71T>C
ENST00000377488.5:c.91-71T>C	ENSP00000366708.1:n.91-71T>C
ENST00000377491.5:c.91-71T>C	ENSP00000366711.1:n.91-71T>C
ENST00000377493.9:c.91-71T>C	ENSP00000466242.1:n.91-71T>C
ENST00000460192.5:n.187-71T>C
ENST00000465354.5:n.160-71T>C
ENST00000493373.5:c.91-71T>C	ENSP00000465404.1:n.91-71T>C
ENST00000493678.5:c.91-71T>C	ENSP00000418770.1:n.91-71T>C
ENST00000497113.1:n.110-71T>C
NM_001123377.1:c.91-71T>C	NP_001116849.1:n.91-71T>C
NM_007262.4:c.91-71T>C	NP_009193.2:n.91-71T>C
XM_005263424.2:c.91-71T>C	XP_005263481.1:n.91-71T>C
XM_005263424.3:c.91-71T>C	XP_005263481.1:n.91-71T>C
NM_007262.5:c.91-71T>C MANE Select	NP_009193.2:n.91-71T>C
NM_001123377.2:c.91-71T>C	NP_001116849.1:n.91-71T>C