Canonical Allele Identifier: CA1152147678
Gene: PARK7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.7985056_7985057delinsGC , CM000663.2:g.7985056_7985057delinsGC GRCh38
NC_000001.10:g.8045116_8045117delinsGC , CM000663.1:g.8045116_8045117delinsGC GRCh37
NC_000001.9:g.7967703_7967704delinsGC NCBI36
NG_008271.1:g.28403_28404delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000338639.10:c.*2_*3delinsGC MANE Select ENSP00000340278.5:n.*2_*3delinsGC
ENST00000338639.9:c.*2_*3delinsGC ENSP00000340278.5:n.*2_*3delinsGC
ENST00000377488.5:c.*2_*3delinsGC ENSP00000366708.1:n.*2_*3delinsGC
ENST00000377491.5:c.*2_*3delinsGC ENSP00000366711.1:n.*2_*3delinsGC
ENST00000377493.9:c.*2_*3delinsGC ENSP00000466242.1:n.*2_*3delinsGC
ENST00000469225.1:c.485_486delinsGC ENSP00000466756.1:n.485_486delinsGC
ENST00000493678.5:c.*2_*3delinsGC ENSP00000418770.1:n.*2_*3delinsGC
NM_001123377.1:c.*2_*3delinsGC NP_001116849.1:n.*2_*3delinsGC
NM_007262.4:c.*2_*3delinsGC NP_009193.2:n.*2_*3delinsGC
XM_005263424.2:c.*2_*3delinsGC XP_005263481.1:n.*2_*3delinsGC
XM_005263424.3:c.*2_*3delinsGC XP_005263481.1:n.*2_*3delinsGC
NM_007262.5:c.*2_*3delinsGC MANE Select NP_009193.2:n.*2_*3delinsGC
NM_001123377.2:c.*2_*3delinsGC NP_001116849.1:n.*2_*3delinsGC