Canonical Allele Identifier: CA2410907359

Gene: SCO2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50525748A= , CM000684.2:g.50525748A=	GRCh38
NC_000022.10:g.50964177A= , CM000684.1:g.50964177A=	GRCh37
NC_000022.9:g.49311043A=	NCBI36
NG_011860.1:g.9338T= , LRG_727:g.9338T=
NG_016235.1:g.5692T=
NG_021419.1:g.22533A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000543927.6:c.-14+498T=	ENSP00000444433.1:n.-14+498T=
ENST00000638598.2:c.-14+253T=	ENSP00000491753.2:n.-14+253T=
ENST00000423348.1:c.-14+498T=	ENSP00000403570.1:n.-14+498T=
ENST00000439934.5:c.-14+253T=	ENSP00000415642.1:n.-14+253T=
ENST00000535425.5:c.-14+253T=	ENSP00000444242.1:n.-14+253T=
ENST00000543927.5:c.-14+498T=	ENSP00000444433.1:n.-14+498T=
NM_001169109.1:c.-14+498T=	NP_001162580.1:n.-14+498T=
NM_001169110.1:c.-14+253T=	NP_001162581.1:n.-14+253T=
NM_001169109.2:c.-14+498T=	NP_001162580.1:n.-14+498T=