Canonical Allele Identifier: CA658080747

Gene: IGLL1

Linked Data

• COSMIC: COSN15589009

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.23573143_23573144insA , CM000684.2:g.23573143_23573144insA	GRCh38
NC_000022.10:g.23915330_23915331insA , CM000684.1:g.23915330_23915331insA	GRCh37
NC_000022.9:g.22245330_22245331insA	NCBI36
NG_009791.1:g.12165_12166insT , LRG_69:g.12165_12166insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330377.3:c.*122_*123insT MANE Select	ENSP00000329312.2:n.*122_*123insT
ENST00000249053.3:c.*393_*394insT	ENSP00000249053.3:n.*393_*394insT
ENST00000330377.2:c.*122_*123insT	ENSP00000329312.2:n.*122_*123insT
NM_020070.3:c.*122_*123insT	NP_064455.1:n.*122_*123insT
NM_152855.2:c.*393_*394insT	NP_690594.1:n.*393_*394insT
XM_011530169.1:c.*122_*123insT	XP_011528471.1:n.*122_*123insT
XM_011530169.2:c.*122_*123insT	XP_011528471.1:n.*122_*123insT
NM_020070.4:c.*122_*123insT MANE Select	NP_064455.1:n.*122_*123insT
NM_001369906.1:c.*122_*123insT	NP_001356835.1:n.*122_*123insT
NM_152855.3:c.*393_*394insT	NP_690594.1:n.*393_*394insT