Canonical Allele Identifier: CA1321413532

Gene: SUMO1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.202236436G= , CM000664.2:g.202236436G=	GRCh38
NC_000002.11:g.203101159G= , CM000664.1:g.203101159G=	GRCh37
NC_000002.10:g.202809404G=	NCBI36
NG_011679.1:g.7164C=

Transcript Alleles

HGVS	Amino-acid Change
NM_003352.8:c.12+2004C= MANE Select	NP_003343.1:n.12+2004C=
ENST00000392246.7:c.12+2004C= MANE Select	ENSP00000376077.2:n.12+2004C=
NM_001005781.1:c.12+2004C=	NP_001005781.1:n.12+2004C=
NM_001005781.2:c.12+2004C=	NP_001005781.1:n.12+2004C=
NM_001005782.1:c.12+2004C=	NP_001005782.1:n.12+2004C=
NM_001005782.2:c.12+2004C=	NP_001005782.1:n.12+2004C=
NM_001371392.1:c.12+2004C=	NP_001358321.1:n.12+2004C=
NM_001371393.1:c.12+2004C=	NP_001358322.1:n.12+2004C=
NM_001371394.1:c.12+2004C=	NP_001358323.1:n.12+2004C=
NM_003352.4:c.12+2004C=	NP_003343.1:n.12+2004C=
NR_163943.1:n.158+2004C=
ENST00000392244.7:c.12+2004C=	ENSP00000376075.3:n.12+2004C=
ENST00000392245.5:c.12+2004C=	ENSP00000376076.1:n.12+2004C=
ENST00000392246.6:c.12+2004C=	ENSP00000376077.2:n.12+2004C=
ENST00000409181.1:c.12+2004C=	ENSP00000386753.1:n.12+2004C=
ENST00000409205.5:c.-101+2004C=	ENSP00000386267.1:n.-101+2004C=
ENST00000409368.5:c.12+2004C=	ENSP00000387204.1:n.12+2004C=
ENST00000409498.6:c.-199+2004C=	ENSP00000386472.2:n.-199+2004C=
ENST00000409627.6:c.12+2004C=	ENSP00000386500.2:n.12+2004C=
ENST00000409712.5:c.12+2004C=	ENSP00000386296.1:n.12+2004C=