Canonical Allele Identifier: CA2643056888

Gene: PARK7

Linked Data

• gnomAD v4: 1-7985090-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.7985090C>A , CM000663.2:g.7985090C>A	GRCh38
NC_000001.10:g.8045150C>A , CM000663.1:g.8045150C>A	GRCh37
NC_000001.9:g.7967737C>A	NCBI36
NG_008271.1:g.28437C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338639.10:c.*36C>A MANE Select	ENSP00000340278.5:n.*36C>A
ENST00000338639.9:c.*36C>A	ENSP00000340278.5:n.*36C>A
ENST00000377488.5:c.*36C>A	ENSP00000366708.1:n.*36C>A
ENST00000377491.5:c.*36C>A	ENSP00000366711.1:n.*36C>A
ENST00000377493.9:c.*36C>A	ENSP00000466242.1:n.*36C>A
ENST00000469225.1:c.519C>A	ENSP00000466756.1:n.519C>A
ENST00000493678.5:c.*36C>A	ENSP00000418770.1:n.*36C>A
NM_001123377.1:c.*36C>A	NP_001116849.1:n.*36C>A
NM_007262.4:c.*36C>A	NP_009193.2:n.*36C>A
XM_005263424.2:c.*36C>A	XP_005263481.1:n.*36C>A
XM_005263424.3:c.*36C>A	XP_005263481.1:n.*36C>A
NM_007262.5:c.*36C>A MANE Select	NP_009193.2:n.*36C>A
NM_001123377.2:c.*36C>A	NP_001116849.1:n.*36C>A