Canonical Allele Identifier: CA569620
Gene: PARK7 HGNC NCBI

Linked Data

dbSNP Id: rs749485971
gnomAD v2: 1-8044975-A-G
gnomAD v3: 1-7984915-A-G
gnomAD v4: 1-7984915-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.7984915A>G , CM000663.2:g.7984915A>G GRCh38
NC_000001.10:g.8044975A>G , CM000663.1:g.8044975A>G GRCh37
NC_000001.9:g.7967562A>G NCBI36
NG_008271.1:g.28262A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000338639.10:c.431A>G MANE Select ENSP00000340278.5:p.Asn144Ser
ENST00000338639.9:c.431A>G ENSP00000340278.5:p.Asn144Ser
ENST00000377488.5:c.431A>G ENSP00000366708.1:p.Asn144Ser
ENST00000377491.5:c.431A>G ENSP00000366711.1:p.Asn144Ser
ENST00000377493.9:c.371A>G ENSP00000466242.1:p.Asn124Ser
ENST00000469225.1:c.344A>G ENSP00000466756.1:p.Asn115Ser
ENST00000493373.5:c.431A>G ENSP00000465404.1:p.Asn144Ser
ENST00000493678.5:c.431A>G ENSP00000418770.1:p.Asn144Ser
NM_001123377.1:c.431A>G NP_001116849.1:p.Asn144Ser
NM_007262.4:c.431A>G NP_009193.2:p.Asn144Ser
XM_005263424.2:c.431A>G XP_005263481.1:p.Asn144Ser
XM_005263424.3:c.431A>G XP_005263481.1:p.Asn144Ser
NM_007262.5:c.431A>G MANE Select NP_009193.2:p.Asn144Ser
NM_001123377.2:c.431A>G NP_001116849.1:p.Asn144Ser