Canonical Allele Identifier: CA2643056889

Gene: PARK7

Linked Data

• gnomAD v4: 1-7985100-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.7985100T>C , CM000663.2:g.7985100T>C	GRCh38
NC_000001.10:g.8045160T>C , CM000663.1:g.8045160T>C	GRCh37
NC_000001.9:g.7967747T>C	NCBI36
NG_008271.1:g.28447T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338639.10:c.*46T>C MANE Select	ENSP00000340278.5:n.*46T>C
ENST00000338639.9:c.*46T>C	ENSP00000340278.5:n.*46T>C
ENST00000377488.5:c.*46T>C	ENSP00000366708.1:n.*46T>C
ENST00000377491.5:c.*46T>C	ENSP00000366711.1:n.*46T>C
ENST00000377493.9:c.*46T>C	ENSP00000466242.1:n.*46T>C
ENST00000469225.1:c.529T>C	ENSP00000466756.1:n.529T>C
ENST00000493678.5:c.*46T>C	ENSP00000418770.1:n.*46T>C
NM_001123377.1:c.*46T>C	NP_001116849.1:n.*46T>C
NM_007262.4:c.*46T>C	NP_009193.2:n.*46T>C
XM_005263424.2:c.*46T>C	XP_005263481.1:n.*46T>C
XM_005263424.3:c.*46T>C	XP_005263481.1:n.*46T>C
NM_007262.5:c.*46T>C MANE Select	NP_009193.2:n.*46T>C
NM_001123377.2:c.*46T>C	NP_001116849.1:n.*46T>C