Canonical Allele Identifier: CA739209045

Gene: PARK7

Linked Data

• dbSNP Id: rs1456528956
• gnomAD v4: 1-7985207-G-A
• MyVariant Identifiers: chr1:g.8045267G>A (hg19) ; chr1:g.7985207G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.7985207G>A , CM000663.2:g.7985207G>A	GRCh38
NC_000001.10:g.8045267G>A , CM000663.1:g.8045267G>A	GRCh37
NC_000001.9:g.7967854G>A	NCBI36
NG_008271.1:g.28554G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338639.10:c.*153G>A MANE Select	ENSP00000340278.5:n.*153G>A
ENST00000338639.9:c.*153G>A	ENSP00000340278.5:n.*153G>A
ENST00000377491.5:c.*153G>A	ENSP00000366711.1:n.*153G>A
ENST00000377493.9:c.*153G>A	ENSP00000466242.1:n.*153G>A
ENST00000469225.1:c.636G>A	ENSP00000466756.1:n.636G>A
ENST00000493678.5:c.*153G>A	ENSP00000418770.1:n.*153G>A
NM_001123377.1:c.*153G>A	NP_001116849.1:n.*153G>A
NM_007262.4:c.*153G>A	NP_009193.2:n.*153G>A
XM_005263424.2:c.*153G>A	XP_005263481.1:n.*153G>A
XM_005263424.3:c.*153G>A	XP_005263481.1:n.*153G>A
NM_007262.5:c.*153G>A MANE Select	NP_009193.2:n.*153G>A
NM_001123377.2:c.*153G>A	NP_001116849.1:n.*153G>A