Canonical Allele Identifier: CA338167171
Gene: PARK7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.7984977G>C , CM000663.2:g.7984977G>C GRCh38
NC_000001.10:g.8045037G>C , CM000663.1:g.8045037G>C GRCh37
NC_000001.9:g.7967624G>C NCBI36
NG_008271.1:g.28324G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000338639.10:c.493G>C MANE Select ENSP00000340278.5:p.Ala165Pro
ENST00000338639.9:c.493G>C ENSP00000340278.5:p.Ala165Pro
ENST00000377488.5:c.493G>C ENSP00000366708.1:p.Ala165Pro
ENST00000377491.5:c.493G>C ENSP00000366711.1:p.Ala165Pro
ENST00000377493.9:c.433G>C ENSP00000466242.1:p.Ala145Pro
ENST00000469225.1:c.406G>C ENSP00000466756.1:p.Ala136Pro
ENST00000493373.5:c.493G>C ENSP00000465404.1:p.Ala165Pro
ENST00000493678.5:c.493G>C ENSP00000418770.1:p.Ala165Pro
NM_001123377.1:c.493G>C NP_001116849.1:p.Ala165Pro
NM_007262.4:c.493G>C NP_009193.2:p.Ala165Pro
XM_005263424.2:c.493G>C XP_005263481.1:p.Ala165Pro
XM_005263424.3:c.493G>C XP_005263481.1:p.Ala165Pro
NM_007262.5:c.493G>C MANE Select NP_009193.2:p.Ala165Pro
NM_001123377.2:c.493G>C NP_001116849.1:p.Ala165Pro