Canonical Allele Identifier: CA1152147813

Gene: PARK7

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.7985110_7985112delinsCTG , CM000663.2:g.7985110_7985112delinsCTG	GRCh38
NC_000001.10:g.8045170_8045172delinsCTG , CM000663.1:g.8045170_8045172delinsCTG	GRCh37
NC_000001.9:g.7967757_7967759delinsCTG	NCBI36
NG_008271.1:g.28457_28459delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338639.10:c.*56_*58delinsCTG MANE Select	ENSP00000340278.5:n.*56_*58delinsCTG
ENST00000338639.9:c.*56_*58delinsCTG	ENSP00000340278.5:n.*56_*58delinsCTG
ENST00000377491.5:c.*56_*58delinsCTG	ENSP00000366711.1:n.*56_*58delinsCTG
ENST00000377493.9:c.*56_*58delinsCTG	ENSP00000466242.1:n.*56_*58delinsCTG
ENST00000469225.1:c.539_541delinsCTG	ENSP00000466756.1:n.539_541delinsCTG
ENST00000493678.5:c.*56_*58delinsCTG	ENSP00000418770.1:n.*56_*58delinsCTG
NM_001123377.1:c.*56_*58delinsCTG	NP_001116849.1:n.*56_*58delinsCTG
NM_007262.4:c.*56_*58delinsCTG	NP_009193.2:n.*56_*58delinsCTG
XM_005263424.2:c.*56_*58delinsCTG	XP_005263481.1:n.*56_*58delinsCTG
XM_005263424.3:c.*56_*58delinsCTG	XP_005263481.1:n.*56_*58delinsCTG
NM_007262.5:c.*56_*58delinsCTG MANE Select	NP_009193.2:n.*56_*58delinsCTG
NM_001123377.2:c.*56_*58delinsCTG	NP_001116849.1:n.*56_*58delinsCTG