Canonical Allele Identifier: CA1140886315

Gene: PARK7

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.7984930A= , CM000663.2:g.7984930A=	GRCh38
NC_000001.10:g.8044990A= , CM000663.1:g.8044990A=	GRCh37
NC_000001.9:g.7967577A=	NCBI36
NG_008271.1:g.28277A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338639.10:c.446A= MANE Select	ENSP00000340278.5:p.Asp149=
ENST00000338639.9:c.446A=	ENSP00000340278.5:p.Asp149=
ENST00000377488.5:c.446A=	ENSP00000366708.1:p.Asp149=
ENST00000377491.5:c.446A=	ENSP00000366711.1:p.Asp149=
ENST00000377493.9:c.386A=	ENSP00000466242.1:p.Asp129=
ENST00000469225.1:c.359A=	ENSP00000466756.1:p.Asp120=
ENST00000493373.5:c.446A=	ENSP00000465404.1:p.Asp149=
ENST00000493678.5:c.446A=	ENSP00000418770.1:p.Asp149=
NM_001123377.1:c.446A=	NP_001116849.1:p.Asp149=
NM_007262.4:c.446A=	NP_009193.2:p.Asp149=
XM_005263424.2:c.446A=	XP_005263481.1:p.Asp149=
XM_005263424.3:c.446A=	XP_005263481.1:p.Asp149=
NM_007262.5:c.446A= MANE Select	NP_009193.2:p.Asp149=
NM_001123377.2:c.446A=	NP_001116849.1:p.Asp149=