Canonical Allele Identifier: CA338167091

Gene: PARK7

Linked Data

• MyVariant Identifiers: chr1:g.8045000T>G (hg19) ; chr1:g.7984940T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.7984940T>G , CM000663.2:g.7984940T>G	GRCh38
NC_000001.10:g.8045000T>G , CM000663.1:g.8045000T>G	GRCh37
NC_000001.9:g.7967587T>G	NCBI36
NG_008271.1:g.28287T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000338639.10:c.456T>G MANE Select	ENSP00000340278.5:p.Ile152Met
ENST00000338639.9:c.456T>G	ENSP00000340278.5:p.Ile152Met
ENST00000377488.5:c.456T>G	ENSP00000366708.1:p.Ile152Met
ENST00000377491.5:c.456T>G	ENSP00000366711.1:p.Ile152Met
ENST00000377493.9:c.396T>G	ENSP00000466242.1:p.Ile132Met
ENST00000469225.1:c.369T>G	ENSP00000466756.1:p.Ile123Met
ENST00000493373.5:c.456T>G	ENSP00000465404.1:p.Ile152Met
ENST00000493678.5:c.456T>G	ENSP00000418770.1:p.Ile152Met
NM_001123377.1:c.456T>G	NP_001116849.1:p.Ile152Met
NM_007262.4:c.456T>G	NP_009193.2:p.Ile152Met
XM_005263424.2:c.456T>G	XP_005263481.1:p.Ile152Met
XM_005263424.3:c.456T>G	XP_005263481.1:p.Ile152Met
NM_007262.5:c.456T>G MANE Select	NP_009193.2:p.Ile152Met
NM_001123377.2:c.456T>G	NP_001116849.1:p.Ile152Met