Canonical Allele Identifier: CA1152147271
Gene: PARK7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.7984838G= , CM000663.2:g.7984838G= GRCh38
NC_000001.10:g.8044898G= , CM000663.1:g.8044898G= GRCh37
NC_000001.9:g.7967485G= NCBI36
NG_008271.1:g.28185G=

Transcript Alleles

HGVS Amino-acid change
ENST00000338639.10:c.410-56G= MANE Select ENSP00000340278.5:n.410-56G=
ENST00000338639.9:c.410-56G= ENSP00000340278.5:n.410-56G=
ENST00000377488.5:c.410-56G= ENSP00000366708.1:n.410-56G=
ENST00000377491.5:c.410-56G= ENSP00000366711.1:n.410-56G=
ENST00000377493.9:c.350-56G= ENSP00000466242.1:n.350-56G=
ENST00000469225.1:c.293-26G= ENSP00000466756.1:n.293-26G=
ENST00000493373.5:c.410-56G= ENSP00000465404.1:n.410-56G=
ENST00000493678.5:c.410-56G= ENSP00000418770.1:n.410-56G=
NM_001123377.1:c.410-56G= NP_001116849.1:n.410-56G=
NM_007262.4:c.410-56G= NP_009193.2:n.410-56G=
XM_005263424.2:c.410-56G= XP_005263481.1:n.410-56G=
XM_005263424.3:c.410-56G= XP_005263481.1:n.410-56G=
NM_007262.5:c.410-56G= MANE Select NP_009193.2:n.410-56G=
NM_001123377.2:c.410-56G= NP_001116849.1:n.410-56G=