Canonical Allele Identifier: CA1152179202

Gene: PARK7

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.7965250_7965251delinsCT , CM000663.2:g.7965250_7965251delinsCT	GRCh38
NC_000001.10:g.8025310_8025311delinsCT , CM000663.1:g.8025310_8025311delinsCT	GRCh37
NC_000001.9:g.7947897_7947898delinsCT	NCBI36
NG_008271.1:g.8597_8598delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338639.10:c.91-74_91-73delinsCT MANE Select	ENSP00000340278.5:n.91-74_91-73delinsCT
ENST00000338639.9:c.91-74_91-73delinsCT	ENSP00000340278.5:n.91-74_91-73delinsCT
ENST00000377488.5:c.91-74_91-73delinsCT	ENSP00000366708.1:n.91-74_91-73delinsCT
ENST00000377491.5:c.91-74_91-73delinsCT	ENSP00000366711.1:n.91-74_91-73delinsCT
ENST00000377493.9:c.91-74_91-73delinsCT	ENSP00000466242.1:n.91-74_91-73delinsCT
ENST00000460192.5:n.187-74_187-73delinsCT
ENST00000465354.5:n.160-74_160-73delinsCT
ENST00000493373.5:c.91-74_91-73delinsCT	ENSP00000465404.1:n.91-74_91-73delinsCT
ENST00000493678.5:c.91-74_91-73delinsCT	ENSP00000418770.1:n.91-74_91-73delinsCT
ENST00000497113.1:n.110-74_110-73delinsCT
NM_001123377.1:c.91-74_91-73delinsCT	NP_001116849.1:n.91-74_91-73delinsCT
NM_007262.4:c.91-74_91-73delinsCT	NP_009193.2:n.91-74_91-73delinsCT
XM_005263424.2:c.91-74_91-73delinsCT	XP_005263481.1:n.91-74_91-73delinsCT
XM_005263424.3:c.91-74_91-73delinsCT	XP_005263481.1:n.91-74_91-73delinsCT
NM_007262.5:c.91-74_91-73delinsCT MANE Select	NP_009193.2:n.91-74_91-73delinsCT
NM_001123377.2:c.91-74_91-73delinsCT	NP_001116849.1:n.91-74_91-73delinsCT