Canonical Allele Identifier: CA14980481
Gene: UBE2L3 HGNC NCBI

Linked Data

dbSNP Id: rs181362

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.21577779C>T , CM000684.2:g.21577779C>T GRCh38
NC_000022.10:g.21932068C>T , CM000684.1:g.21932068C>T GRCh37
NC_000022.9:g.20262068C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000696046.1:c.27+10008C>T ENSP00000512350.1:n.27+10008C>T
ENST00000342192.9:c.27+10008C>T MANE Select ENSP00000344259.5:n.27+10008C>T
ENST00000342192.8:c.27+10008C>T ENSP00000344259.4:n.27+10008C>T
ENST00000458578.6:c.202-15082C>T ENSP00000400906.2:n.202-15082C>T
ENST00000496722.1:n.648+9402C>T
ENST00000545681.2:c.27+10008C>T ENSP00000445931.1:n.27+10008C>T
NM_001256355.1:c.202-15082C>T NP_001243284.1:n.202-15082C>T
NM_001256356.1:c.27+10008C>T NP_001243285.1:n.27+10008C>T
NM_003347.3:c.27+10008C>T NP_003338.1:n.27+10008C>T
NR_028436.2:n.225+10008C>T
NR_046082.1:n.648+9402C>T
XM_017028935.2:c.27+10008C>T XP_016884424.1:n.27+10008C>T
NM_003347.4:c.27+10008C>T MANE Select NP_003338.1:n.27+10008C>T
NR_028436.3:n.58+10008C>T
NR_046082.2:n.664+9402C>T
NM_001256356.2:c.27+10008C>T NP_001243285.1:n.27+10008C>T