Canonical Allele Identifier: CA1152147771

Gene: PARK7

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.7985091_7985092delinsCG , CM000663.2:g.7985091_7985092delinsCG	GRCh38
NC_000001.10:g.8045151_8045152delinsCG , CM000663.1:g.8045151_8045152delinsCG	GRCh37
NC_000001.9:g.7967738_7967739delinsCG	NCBI36
NG_008271.1:g.28438_28439delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338639.10:c.*37_*38delinsCG MANE Select	ENSP00000340278.5:n.*37_*38delinsCG
ENST00000338639.9:c.*37_*38delinsCG	ENSP00000340278.5:n.*37_*38delinsCG
ENST00000377488.5:c.*37_*38delinsCG	ENSP00000366708.1:n.*37_*38delinsCG
ENST00000377491.5:c.*37_*38delinsCG	ENSP00000366711.1:n.*37_*38delinsCG
ENST00000377493.9:c.*37_*38delinsCG	ENSP00000466242.1:n.*37_*38delinsCG
ENST00000469225.1:c.520_521delinsCG	ENSP00000466756.1:n.520_521delinsCG
ENST00000493678.5:c.*37_*38delinsCG	ENSP00000418770.1:n.*37_*38delinsCG
NM_001123377.1:c.*37_*38delinsCG	NP_001116849.1:n.*37_*38delinsCG
NM_007262.4:c.*37_*38delinsCG	NP_009193.2:n.*37_*38delinsCG
XM_005263424.2:c.*37_*38delinsCG	XP_005263481.1:n.*37_*38delinsCG
XM_005263424.3:c.*37_*38delinsCG	XP_005263481.1:n.*37_*38delinsCG
NM_007262.5:c.*37_*38delinsCG MANE Select	NP_009193.2:n.*37_*38delinsCG
NM_001123377.2:c.*37_*38delinsCG	NP_001116849.1:n.*37_*38delinsCG