Canonical Allele Identifier: CA16000866

Gene: UBE2L3

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.21610472G>A , CM000684.2:g.21610472G>A	GRCh38
NC_000022.10:g.21964761G>A , CM000684.1:g.21964761G>A	GRCh37
NC_000022.9:g.20294761G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696046.1:c.124-385G>A	ENSP00000512350.1:n.124-385G>A
ENST00000342192.9:c.124-385G>A MANE Select	ENSP00000344259.5:n.124-385G>A
ENST00000342192.8:c.124-385G>A	ENSP00000344259.4:n.124-385G>A
ENST00000458578.6:c.298-385G>A	ENSP00000400906.2:n.298-385G>A
ENST00000496722.1:n.745-385G>A
ENST00000545681.2:c.28-385G>A	ENSP00000445931.1:n.28-385G>A
NM_001256355.1:c.298-385G>A	NP_001243284.1:n.298-385G>A
NM_001256356.1:c.28-385G>A	NP_001243285.1:n.28-385G>A
NM_003347.3:c.124-385G>A	NP_003338.1:n.124-385G>A
NR_028436.2:n.322-385G>A
NR_046082.1:n.745-385G>A
XM_017028935.2:c.124-385G>A	XP_016884424.1:n.124-385G>A
NM_003347.4:c.124-385G>A MANE Select	NP_003338.1:n.124-385G>A
NR_028436.3:n.155-385G>A
NR_046082.2:n.761-385G>A
NM_001256356.2:c.28-385G>A	NP_001243285.1:n.28-385G>A