Canonical Allele Identifier: CA521019996

Gene: PARK7

Linked Data

• dbSNP Id: rs777064688
• gnomAD v2: 1-8045149-G-A
• gnomAD v4: 1-7985089-G-A
• MyVariant Identifiers: chr1:g.8045149G>A (hg19) ; chr1:g.7985089G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.7985089G>A , CM000663.2:g.7985089G>A	GRCh38
NC_000001.10:g.8045149G>A , CM000663.1:g.8045149G>A	GRCh37
NC_000001.9:g.7967736G>A	NCBI36
NG_008271.1:g.28436G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338639.10:c.*35G>A MANE Select	ENSP00000340278.5:n.*35G>A
ENST00000338639.9:c.*35G>A	ENSP00000340278.5:n.*35G>A
ENST00000377488.5:c.*35G>A	ENSP00000366708.1:n.*35G>A
ENST00000377491.5:c.*35G>A	ENSP00000366711.1:n.*35G>A
ENST00000377493.9:c.*35G>A	ENSP00000466242.1:n.*35G>A
ENST00000469225.1:c.518G>A	ENSP00000466756.1:n.518G>A
ENST00000493678.5:c.*35G>A	ENSP00000418770.1:n.*35G>A
NM_001123377.1:c.*35G>A	NP_001116849.1:n.*35G>A
NM_007262.4:c.*35G>A	NP_009193.2:n.*35G>A
XM_005263424.2:c.*35G>A	XP_005263481.1:n.*35G>A
XM_005263424.3:c.*35G>A	XP_005263481.1:n.*35G>A
NM_007262.5:c.*35G>A MANE Select	NP_009193.2:n.*35G>A
NM_001123377.2:c.*35G>A	NP_001116849.1:n.*35G>A