Canonical Allele Identifier: CA17286829

Gene: PARK7

Linked Data

• dbSNP Id: rs562641550
• gnomAD v3: 1-7985169-C-T
• gnomAD v4: 1-7985169-C-T
• MyVariant Identifiers: chr1:g.8045229C>T (hg19) ; chr1:g.7985169C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.7985169C>T , CM000663.2:g.7985169C>T	GRCh38
NC_000001.10:g.8045229C>T , CM000663.1:g.8045229C>T	GRCh37
NC_000001.9:g.7967816C>T	NCBI36
NG_008271.1:g.28516C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338639.10:c.*115C>T MANE Select	ENSP00000340278.5:n.*115C>T
ENST00000338639.9:c.*115C>T	ENSP00000340278.5:n.*115C>T
ENST00000377491.5:c.*115C>T	ENSP00000366711.1:n.*115C>T
ENST00000377493.9:c.*115C>T	ENSP00000466242.1:n.*115C>T
ENST00000469225.1:c.598C>T	ENSP00000466756.1:n.598C>T
ENST00000493678.5:c.*115C>T	ENSP00000418770.1:n.*115C>T
NM_001123377.1:c.*115C>T	NP_001116849.1:n.*115C>T
NM_007262.4:c.*115C>T	NP_009193.2:n.*115C>T
XM_005263424.2:c.*115C>T	XP_005263481.1:n.*115C>T
XM_005263424.3:c.*115C>T	XP_005263481.1:n.*115C>T
NM_007262.5:c.*115C>T MANE Select	NP_009193.2:n.*115C>T
NM_001123377.2:c.*115C>T	NP_001116849.1:n.*115C>T