Canonical Allele Identifier: CA15166057
Gene: SUMO1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.202224545G>A , CM000664.2:g.202224545G>A GRCh38
NC_000002.11:g.203089268G>A , CM000664.1:g.203089268G>A GRCh37
NC_000002.10:g.202797513G>A NCBI36
NG_011679.1:g.19055C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000392246.7:c.13-4439C>T MANE Select ENSP00000376077.2:n.13-4439C>T
ENST00000392244.7:c.13-10111C>T ENSP00000376075.3:n.13-10111C>T
ENST00000392245.5:c.13-4439C>T ENSP00000376076.1:n.13-4439C>T
ENST00000392246.6:c.13-4439C>T ENSP00000376077.2:n.13-4439C>T
ENST00000409181.1:c.13-4439C>T ENSP00000386753.1:n.13-4439C>T
ENST00000409205.5:c.-100-4439C>T ENSP00000386267.1:n.-100-4439C>T
ENST00000409368.5:c.13-4439C>T ENSP00000387204.1:n.13-4439C>T
ENST00000409498.6:c.-105-4439C>T ENSP00000386472.2:n.-105-4439C>T
ENST00000409627.6:c.203-4439C>T ENSP00000386500.2:n.203-4439C>T
ENST00000409712.5:c.13-4439C>T ENSP00000386296.1:n.13-4439C>T
NM_001005781.1:c.13-4439C>T NP_001005781.1:n.13-4439C>T
NM_001005782.1:c.13-10111C>T NP_001005782.1:n.13-10111C>T
NM_003352.4:c.13-4439C>T NP_003343.1:n.13-4439C>T
NM_001005781.2:c.13-4439C>T NP_001005781.1:n.13-4439C>T
NM_001005782.2:c.13-10111C>T NP_001005782.1:n.13-10111C>T
NM_001371392.1:c.13-4442C>T NP_001358321.1:n.13-4442C>T
NM_001371393.1:c.13-4439C>T NP_001358322.1:n.13-4439C>T
NM_001371394.1:c.13-4439C>T NP_001358323.1:n.13-4439C>T
NM_003352.8:c.13-4439C>T MANE Select NP_003343.1:n.13-4439C>T
NR_163943.1:n.159-4439C>T
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