Canonical Allele Identifier: CA2643056957

Gene: PARK7

Linked Data

• gnomAD v4: 1-7985221-CAA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.7985223_7985224del , CM000663.2:g.7985223_7985224del	GRCh38
NC_000001.10:g.8045283_8045284del , CM000663.1:g.8045283_8045284del	GRCh37
NC_000001.9:g.7967870_7967871del	NCBI36
NG_008271.1:g.28570_28571del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338639.10:c.*169_*170del MANE Select	ENSP00000340278.5:n.*169_*170del
ENST00000338639.9:c.*169_*170del	ENSP00000340278.5:n.*169_*170del
ENST00000377491.5:c.*169_*170del	ENSP00000366711.1:n.*169_*170del
ENST00000377493.9:c.*169_*170del	ENSP00000466242.1:n.*169_*170del
ENST00000469225.1:c.652_653del	ENSP00000466756.1:n.652_653del
ENST00000493678.5:c.*169_*170del	ENSP00000418770.1:n.*169_*170del
NM_001123377.1:c.*169_*170del	NP_001116849.1:n.*169_*170del
NM_007262.4:c.*169_*170del	NP_009193.2:n.*169_*170del
XM_005263424.2:c.*169_*170del	XP_005263481.1:n.*169_*170del
XM_005263424.3:c.*169_*170del	XP_005263481.1:n.*169_*170del
NM_007262.5:c.*169_*170del MANE Select	NP_009193.2:n.*169_*170del
NM_001123377.2:c.*169_*170del	NP_001116849.1:n.*169_*170del