Canonical Allele Identifier: CA1152147943

Gene: PARK7

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.7985203_7985205delinsCAG , CM000663.2:g.7985203_7985205delinsCAG	GRCh38
NC_000001.10:g.8045263_8045265delinsCAG , CM000663.1:g.8045263_8045265delinsCAG	GRCh37
NC_000001.9:g.7967850_7967852delinsCAG	NCBI36
NG_008271.1:g.28550_28552delinsCAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338639.10:c.*149_*151delinsCAG MANE Select	ENSP00000340278.5:n.*149_*151delinsCAG
ENST00000338639.9:c.*149_*151delinsCAG	ENSP00000340278.5:n.*149_*151delinsCAG
ENST00000377491.5:c.*149_*151delinsCAG	ENSP00000366711.1:n.*149_*151delinsCAG
ENST00000377493.9:c.*149_*151delinsCAG	ENSP00000466242.1:n.*149_*151delinsCAG
ENST00000469225.1:c.632_634delinsCAG	ENSP00000466756.1:n.632_634delinsCAG
ENST00000493678.5:c.*149_*151delinsCAG	ENSP00000418770.1:n.*149_*151delinsCAG
NM_001123377.1:c.*149_*151delinsCAG	NP_001116849.1:n.*149_*151delinsCAG
NM_007262.4:c.*149_*151delinsCAG	NP_009193.2:n.*149_*151delinsCAG
XM_005263424.2:c.*149_*151delinsCAG	XP_005263481.1:n.*149_*151delinsCAG
XM_005263424.3:c.*149_*151delinsCAG	XP_005263481.1:n.*149_*151delinsCAG
NM_007262.5:c.*149_*151delinsCAG MANE Select	NP_009193.2:n.*149_*151delinsCAG
NM_001123377.2:c.*149_*151delinsCAG	NP_001116849.1:n.*149_*151delinsCAG