Canonical Allele Identifier: CA415839004
Gene: PARK7 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.8044970T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.7984910T>A , CM000663.2:g.7984910T>A GRCh38
NC_000001.10:g.8044970T>A , CM000663.1:g.8044970T>A GRCh37
NC_000001.9:g.7967557T>A NCBI36
NG_008271.1:g.28257T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000338639.10:c.426T>A MANE Select ENSP00000340278.5:p.Ser142=
ENST00000338639.9:c.426T>A ENSP00000340278.5:p.Ser142=
ENST00000377488.5:c.426T>A ENSP00000366708.1:p.Ser142=
ENST00000377491.5:c.426T>A ENSP00000366711.1:p.Ser142=
ENST00000377493.9:c.366T>A ENSP00000466242.1:p.Ser122=
ENST00000469225.1:c.339T>A ENSP00000466756.1:p.Ser113=
ENST00000493373.5:c.426T>A ENSP00000465404.1:p.Ser142=
ENST00000493678.5:c.426T>A ENSP00000418770.1:p.Ser142=
NM_001123377.1:c.426T>A NP_001116849.1:p.Ser142=
NM_007262.4:c.426T>A NP_009193.2:p.Ser142=
XM_005263424.2:c.426T>A XP_005263481.1:p.Ser142=
XM_005263424.3:c.426T>A XP_005263481.1:p.Ser142=
NM_007262.5:c.426T>A MANE Select NP_009193.2:p.Ser142=
NM_001123377.2:c.426T>A NP_001116849.1:p.Ser142=