Canonical Allele Identifier: CA2643056870

Gene: PARK7

Linked Data

• dbSNP Id: rs2124005749
• gnomAD v4: 1-7984873-TTTTCTG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.7984879_7984884del , CM000663.2:g.7984879_7984884del	GRCh38
NC_000001.10:g.8044939_8044944del , CM000663.1:g.8044939_8044944del	GRCh37
NC_000001.9:g.7967526_7967531del	NCBI36
NG_008271.1:g.28226_28231del

Transcript Alleles

HGVS	Amino-acid change
ENST00000338639.10:c.410-15_410-10del MANE Select	ENSP00000340278.5:n.410-15_410-10del
ENST00000338639.9:c.410-15_410-10del	ENSP00000340278.5:n.410-15_410-10del
ENST00000377488.5:c.410-15_410-10del	ENSP00000366708.1:n.410-15_410-10del
ENST00000377491.5:c.410-15_410-10del	ENSP00000366711.1:n.410-15_410-10del
ENST00000377493.9:c.350-15_350-10del	ENSP00000466242.1:n.350-15_350-10del
ENST00000469225.1:c.308_313del	ENSP00000466756.1:p.Cys103_Phe104del
ENST00000493373.5:c.410-15_410-10del	ENSP00000465404.1:n.410-15_410-10del
ENST00000493678.5:c.410-15_410-10del	ENSP00000418770.1:n.410-15_410-10del
NM_001123377.1:c.410-15_410-10del	NP_001116849.1:n.410-15_410-10del
NM_007262.4:c.410-15_410-10del	NP_009193.2:n.410-15_410-10del
XM_005263424.2:c.410-15_410-10del	XP_005263481.1:n.410-15_410-10del
XM_005263424.3:c.410-15_410-10del	XP_005263481.1:n.410-15_410-10del
NM_007262.5:c.410-15_410-10del MANE Select	NP_009193.2:n.410-15_410-10del
NM_001123377.2:c.410-15_410-10del	NP_001116849.1:n.410-15_410-10del