Canonical Allele Identifier: CA2396198177

Gene: DGCR8

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.20110836T= , CM000684.2:g.20110836T=	GRCh38
NC_000022.10:g.20098359T= , CM000684.1:g.20098359T=	GRCh37
NC_000022.9:g.18478359T=	NCBI36
NG_022931.1:g.35605T=
NG_022931.2:g.35605T=

Transcript Alleles

HGVS	Amino-acid Change
NM_022720.7:c.*728T= MANE Select	NP_073557.3:n.*728T=
ENST00000351989.8:c.*728T= MANE Select	ENSP00000263209.3:n.*728T=
NM_001190326.1:c.*728T=	NP_001177255.1:n.*728T=
NM_001190326.2:c.*728T=	NP_001177255.1:n.*728T=
NM_022720.6:c.*728T=	NP_073557.3:n.*728T=
ENST00000351989.7:c.*728T=	ENSP00000263209.3:n.*728T=
ENST00000383024.6:c.*728T=	ENSP00000372488.2:n.*728T=
ENST00000407755.1:c.*728T=	ENSP00000384726.1:n.*728T=
ENST00000407755.2:c.*728T=	ENSP00000384726.1:n.*728T=
ENST00000457069.2:c.*728T=	ENSP00000409625.2:n.*728T=
ENST00000475941.1:n.2244T=
ENST00000495826.5:n.3659T=
ENST00000498171.5:n.2620T=
ENST00000704820.1:c.*728T=	ENSP00000516052.1:n.*728T=
ENST00000704821.1:c.*728T=	ENSP00000516053.1:n.*728T=
XM_006724268.2:c.*728T=	XP_006724331.1:n.*728T=
XM_006724268.3:c.*728T=	XP_006724331.1:n.*728T=