Canonical Allele Identifier: CA338166940

Gene: PARK7

Linked Data

• MyVariant Identifiers: chr1:g.8044932C>T (hg19) ; chr1:g.7984872C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.7984872C>T , CM000663.2:g.7984872C>T	GRCh38
NC_000001.10:g.8044932C>T , CM000663.1:g.8044932C>T	GRCh37
NC_000001.9:g.7967519C>T	NCBI36
NG_008271.1:g.28219C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000338639.10:c.410-22C>T MANE Select	ENSP00000340278.5:n.410-22C>T
ENST00000338639.9:c.410-22C>T	ENSP00000340278.5:n.410-22C>T
ENST00000377488.5:c.410-22C>T	ENSP00000366708.1:n.410-22C>T
ENST00000377491.5:c.410-22C>T	ENSP00000366711.1:n.410-22C>T
ENST00000377493.9:c.350-22C>T	ENSP00000466242.1:n.350-22C>T
ENST00000469225.1:c.301C>T	ENSP00000466756.1:p.Leu101Phe
ENST00000493373.5:c.410-22C>T	ENSP00000465404.1:n.410-22C>T
ENST00000493678.5:c.410-22C>T	ENSP00000418770.1:n.410-22C>T
NM_001123377.1:c.410-22C>T	NP_001116849.1:n.410-22C>T
NM_007262.4:c.410-22C>T	NP_009193.2:n.410-22C>T
XM_005263424.2:c.410-22C>T	XP_005263481.1:n.410-22C>T
XM_005263424.3:c.410-22C>T	XP_005263481.1:n.410-22C>T
NM_007262.5:c.410-22C>T MANE Select	NP_009193.2:n.410-22C>T
NM_001123377.2:c.410-22C>T	NP_001116849.1:n.410-22C>T