Canonical Allele Identifier: CA1152147961

Gene: PARK7

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.7985225_7985227delinsTTG , CM000663.2:g.7985225_7985227delinsTTG	GRCh38
NC_000001.10:g.8045285_8045287delinsTTG , CM000663.1:g.8045285_8045287delinsTTG	GRCh37
NC_000001.9:g.7967872_7967874delinsTTG	NCBI36
NG_008271.1:g.28572_28574delinsTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338639.10:c.*171_*173delinsTTG MANE Select	ENSP00000340278.5:n.*171_*173delinsTTG
ENST00000338639.9:c.*171_*173delinsTTG	ENSP00000340278.5:n.*171_*173delinsTTG
ENST00000377491.5:c.*171_*173delinsTTG	ENSP00000366711.1:n.*171_*173delinsTTG
ENST00000377493.9:c.*171_*173delinsTTG	ENSP00000466242.1:n.*171_*173delinsTTG
ENST00000469225.1:c.654_656delinsTTG	ENSP00000466756.1:n.654_656delinsTTG
ENST00000493678.5:c.*171_*173delinsTTG	ENSP00000418770.1:n.*171_*173delinsTTG
NM_001123377.1:c.*171_*173delinsTTG	NP_001116849.1:n.*171_*173delinsTTG
NM_007262.4:c.*171_*173delinsTTG	NP_009193.2:n.*171_*173delinsTTG
XM_005263424.2:c.*171_*173delinsTTG	XP_005263481.1:n.*171_*173delinsTTG
XM_005263424.3:c.*171_*173delinsTTG	XP_005263481.1:n.*171_*173delinsTTG
NM_007262.5:c.*171_*173delinsTTG MANE Select	NP_009193.2:n.*171_*173delinsTTG
NM_001123377.2:c.*171_*173delinsTTG	NP_001116849.1:n.*171_*173delinsTTG