Canonical Allele Identifier: CA14980485

Gene: UBE2L3

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.21619030C>T , CM000684.2:g.21619030C>T	GRCh38
NC_000022.10:g.21973319C>T , CM000684.1:g.21973319C>T	GRCh37
NC_000022.9:g.20303319C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696046.1:c.*54-2485C>T	ENSP00000512350.1:n.*54-2485C>T
ENST00000342192.9:c.311-2485C>T MANE Select	ENSP00000344259.5:n.311-2485C>T
ENST00000342192.8:c.311-2485C>T	ENSP00000344259.4:n.311-2485C>T
ENST00000458578.6:c.485-2485C>T	ENSP00000400906.2:n.485-2485C>T
ENST00000496722.1:n.932-2485C>T
ENST00000545681.2:c.215-2485C>T	ENSP00000445931.1:n.215-2485C>T
NM_001256355.1:c.485-2485C>T	NP_001243284.1:n.485-2485C>T
NM_001256356.1:c.215-2485C>T	NP_001243285.1:n.215-2485C>T
NM_003347.3:c.311-2485C>T	NP_003338.1:n.311-2485C>T
NR_028436.2:n.618-2485C>T
NR_046082.1:n.932-2485C>T
NM_003347.4:c.311-2485C>T MANE Select	NP_003338.1:n.311-2485C>T
NR_028436.3:n.451-2485C>T
NR_046082.2:n.948-2485C>T
NM_001256356.2:c.215-2485C>T	NP_001243285.1:n.215-2485C>T