Canonical Allele Identifier: CA763423080

Gene: SUMO1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.202214584T>A , CM000664.2:g.202214584T>A	GRCh38
NC_000002.11:g.203079307T>A , CM000664.1:g.203079307T>A	GRCh37
NC_000002.10:g.202787552T>A	NCBI36
NG_011679.1:g.29016A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392246.7:c.88-150A>T MANE Select	ENSP00000376077.2:n.88-150A>T
ENST00000392244.7:c.13-150A>T	ENSP00000376075.3:n.13-150A>T
ENST00000392245.5:c.88-150A>T	ENSP00000376076.1:n.88-150A>T
ENST00000392246.6:c.88-150A>T	ENSP00000376077.2:n.88-150A>T
ENST00000409181.1:c.88-150A>T	ENSP00000386753.1:n.88-150A>T
ENST00000409205.5:c.-25-155A>T	ENSP00000386267.1:n.-25-155A>T
ENST00000409368.5:c.88-150A>T	ENSP00000387204.1:n.88-150A>T
ENST00000409498.6:c.-30-150A>T	ENSP00000386472.2:n.-30-150A>T
ENST00000409627.6:c.*56-150A>T	ENSP00000386500.2:n.*56-150A>T
ENST00000409712.5:c.88-150A>T	ENSP00000386296.1:n.88-150A>T
ENST00000469034.1:n.286-150A>T
NM_001005781.1:c.88-150A>T	NP_001005781.1:n.88-150A>T
NM_001005782.1:c.13-150A>T	NP_001005782.1:n.13-150A>T
NM_003352.4:c.88-150A>T	NP_003343.1:n.88-150A>T
NM_001005781.2:c.88-150A>T	NP_001005781.1:n.88-150A>T
NM_001005782.2:c.13-150A>T	NP_001005782.1:n.13-150A>T
NM_001371392.1:c.85-150A>T	NP_001358321.1:n.85-150A>T
NM_001371393.1:c.88-150A>T	NP_001358322.1:n.88-150A>T
NM_001371394.1:c.88-150A>T	NP_001358323.1:n.88-150A>T
NM_003352.8:c.88-150A>T MANE Select	NP_003343.1:n.88-150A>T
NR_163943.1:n.234-150A>T