Canonical Allele Identifier: CA2643056866

Gene: PARK7

Linked Data

• gnomAD v4: 1-7984855-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.7984855G>T , CM000663.2:g.7984855G>T	GRCh38
NC_000001.10:g.8044915G>T , CM000663.1:g.8044915G>T	GRCh37
NC_000001.9:g.7967502G>T	NCBI36
NG_008271.1:g.28202G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000338639.10:c.410-39G>T MANE Select	ENSP00000340278.5:n.410-39G>T
ENST00000338639.9:c.410-39G>T	ENSP00000340278.5:n.410-39G>T
ENST00000377488.5:c.410-39G>T	ENSP00000366708.1:n.410-39G>T
ENST00000377491.5:c.410-39G>T	ENSP00000366711.1:n.410-39G>T
ENST00000377493.9:c.350-39G>T	ENSP00000466242.1:n.350-39G>T
ENST00000469225.1:c.293-9G>T	ENSP00000466756.1:n.293-9G>T
ENST00000493373.5:c.410-39G>T	ENSP00000465404.1:n.410-39G>T
ENST00000493678.5:c.410-39G>T	ENSP00000418770.1:n.410-39G>T
NM_001123377.1:c.410-39G>T	NP_001116849.1:n.410-39G>T
NM_007262.4:c.410-39G>T	NP_009193.2:n.410-39G>T
XM_005263424.2:c.410-39G>T	XP_005263481.1:n.410-39G>T
XM_005263424.3:c.410-39G>T	XP_005263481.1:n.410-39G>T
NM_007262.5:c.410-39G>T MANE Select	NP_009193.2:n.410-39G>T
NM_001123377.2:c.410-39G>T	NP_001116849.1:n.410-39G>T