Canonical Allele Identifier: CA2643056944
Gene: PARK7 HGNC NCBI

Linked Data

gnomAD v4: 1-7985204-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.7985204A>C , CM000663.2:g.7985204A>C GRCh38
NC_000001.10:g.8045264A>C , CM000663.1:g.8045264A>C GRCh37
NC_000001.9:g.7967851A>C NCBI36
NG_008271.1:g.28551A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000338639.10:c.*150A>C MANE Select ENSP00000340278.5:n.*150A>C
ENST00000338639.9:c.*150A>C ENSP00000340278.5:n.*150A>C
ENST00000377491.5:c.*150A>C ENSP00000366711.1:n.*150A>C
ENST00000377493.9:c.*150A>C ENSP00000466242.1:n.*150A>C
ENST00000469225.1:c.633A>C ENSP00000466756.1:n.633A>C
ENST00000493678.5:c.*150A>C ENSP00000418770.1:n.*150A>C
NM_001123377.1:c.*150A>C NP_001116849.1:n.*150A>C
NM_007262.4:c.*150A>C NP_009193.2:n.*150A>C
XM_005263424.2:c.*150A>C XP_005263481.1:n.*150A>C
XM_005263424.3:c.*150A>C XP_005263481.1:n.*150A>C
NM_007262.5:c.*150A>C MANE Select NP_009193.2:n.*150A>C
NM_001123377.2:c.*150A>C NP_001116849.1:n.*150A>C