Canonical Allele Identifier: CA10610775
Gene: PARK7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.7961737T>A , CM000663.2:g.7961737T>A GRCh38
NC_000001.10:g.8021797T>A , CM000663.1:g.8021797T>A GRCh37
NC_000001.9:g.7944384T>A NCBI36
NG_008271.1:g.5084T>A

Transcript Alleles

HGVS Amino-acid Change
NM_007262.5:c.-80T>A MANE Select NP_009193.2:n.-80T>A
ENST00000338639.10:c.-80T>A MANE Select ENSP00000340278.5:n.-80T>A
NM_001123377.1:c.-24+2T>A NP_001116849.1:n.-24+2T>A
NM_001123377.2:c.-24+2T>A NP_001116849.1:n.-24+2T>A
NM_007262.4:c.-80T>A NP_009193.2:n.-80T>A
ENST00000338639.9:c.-80T>A ENSP00000340278.5:n.-80T>A
ENST00000377493.9:c.-24+2T>A ENSP00000466242.1:n.-24+2T>A
ENST00000460192.5:n.73+2T>A
ENST00000493373.5:c.-23-1026T>A ENSP00000465404.1:n.-23-1026T>A
ENST00000493678.5:c.-24+2T>A ENSP00000418770.1:n.-24+2T>A