Canonical Allele Identifier: CA1152147877

Gene: PARK7

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.7985150_7985151delinsTC , CM000663.2:g.7985150_7985151delinsTC	GRCh38
NC_000001.10:g.8045210_8045211delinsTC , CM000663.1:g.8045210_8045211delinsTC	GRCh37
NC_000001.9:g.7967797_7967798delinsTC	NCBI36
NG_008271.1:g.28497_28498delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338639.10:c.*96_*97delinsTC MANE Select	ENSP00000340278.5:n.*96_*97delinsTC
ENST00000338639.9:c.*96_*97delinsTC	ENSP00000340278.5:n.*96_*97delinsTC
ENST00000377491.5:c.*96_*97delinsTC	ENSP00000366711.1:n.*96_*97delinsTC
ENST00000377493.9:c.*96_*97delinsTC	ENSP00000466242.1:n.*96_*97delinsTC
ENST00000469225.1:c.579_580delinsTC	ENSP00000466756.1:n.579_580delinsTC
ENST00000493678.5:c.*96_*97delinsTC	ENSP00000418770.1:n.*96_*97delinsTC
NM_001123377.1:c.*96_*97delinsTC	NP_001116849.1:n.*96_*97delinsTC
NM_007262.4:c.*96_*97delinsTC	NP_009193.2:n.*96_*97delinsTC
XM_005263424.2:c.*96_*97delinsTC	XP_005263481.1:n.*96_*97delinsTC
XM_005263424.3:c.*96_*97delinsTC	XP_005263481.1:n.*96_*97delinsTC
NM_007262.5:c.*96_*97delinsTC MANE Select	NP_009193.2:n.*96_*97delinsTC
NM_001123377.2:c.*96_*97delinsTC	NP_001116849.1:n.*96_*97delinsTC