Canonical Allele Identifier: CA569668

Gene: PARK7

Linked Data

• dbSNP Id: rs375081848
• ExAC: 1:8045152 G / A
• gnomAD v2: 1-8045152-G-A
• gnomAD v3: 1-7985092-G-A
• gnomAD v4: 1-7985092-G-A
• MyVariant Identifiers: chr1:g.8045152G>A (hg19) ; chr1:g.7985092G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.7985092G>A , CM000663.2:g.7985092G>A	GRCh38
NC_000001.10:g.8045152G>A , CM000663.1:g.8045152G>A	GRCh37
NC_000001.9:g.7967739G>A	NCBI36
NG_008271.1:g.28439G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338639.10:c.*38G>A MANE Select	ENSP00000340278.5:n.*38G>A
ENST00000338639.9:c.*38G>A	ENSP00000340278.5:n.*38G>A
ENST00000377488.5:c.*38G>A	ENSP00000366708.1:n.*38G>A
ENST00000377491.5:c.*38G>A	ENSP00000366711.1:n.*38G>A
ENST00000377493.9:c.*38G>A	ENSP00000466242.1:n.*38G>A
ENST00000469225.1:c.521G>A	ENSP00000466756.1:n.521G>A
ENST00000493678.5:c.*38G>A	ENSP00000418770.1:n.*38G>A
NM_001123377.1:c.*38G>A	NP_001116849.1:n.*38G>A
NM_007262.4:c.*38G>A	NP_009193.2:n.*38G>A
XM_005263424.2:c.*38G>A	XP_005263481.1:n.*38G>A
XM_005263424.3:c.*38G>A	XP_005263481.1:n.*38G>A
NM_007262.5:c.*38G>A MANE Select	NP_009193.2:n.*38G>A
NM_001123377.2:c.*38G>A	NP_001116849.1:n.*38G>A