Canonical Allele Identifier: CA2308738110

Gene: KDSR

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.63362727C= , CM000680.2:g.63362727C=	GRCh38
NC_000018.9:g.61029960C= , CM000680.1:g.61029960C=	GRCh37
NC_000018.8:g.59180940C=	NCBI36
NG_028249.1:g.9547G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000591902.6:c.198+52G=	ENSP00000468203.2:n.198+52G=
ENST00000644624.1:c.*137+52G=	ENSP00000494878.1:n.*137+52G=
ENST00000645214.2:c.198+52G= MANE Select	ENSP00000494352.1:n.198+52G=
ENST00000646205.1:c.*348+52G=	ENSP00000496260.1:n.*348+52G=
ENST00000326575.9:c.198+52G=	ENSP00000312939.5:n.198+52G=
ENST00000406396.7:c.198+52G=	ENSP00000385083.2:n.198+52G=
ENST00000585456.1:n.208+52G=
ENST00000589530.5:n.283+52G=
ENST00000592327.1:c.198+52G=	ENSP00000467962.1:n.198+52G=
NM_002035.2:c.198+52G=	NP_002026.1:n.198+52G=
XM_005266677.1:c.198+52G=	XP_005266734.1:n.198+52G=
XM_006722433.2:c.111+52G=	XP_006722496.1:n.111+52G=
NM_002035.4:c.198+52G= MANE Select	NP_002026.1:n.198+52G=
XM_005266677.3:c.198+52G=	XP_005266734.1:n.198+52G=
XM_017025690.2:c.-34+52G=	XP_016881179.1:n.-34+52G=