Canonical Allele Identifier: CA2397855759

Gene: IGLL1

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.23573169_23573185delinsCAGGGAGAAGGGCTGGA , CM000684.2:g.23573169_23573185delinsCAGGGAGAAGGGCTGGA	GRCh38
NC_000022.10:g.23915356_23915372delinsCAGGGAGAAGGGCTGGA , CM000684.1:g.23915356_23915372delinsCAGGGAGAAGGGCTGGA	GRCh37
NC_000022.9:g.22245356_22245372delinsCAGGGAGAAGGGCTGGA	NCBI36
NG_009791.1:g.12124_12140delinsTCCAGCCCTTCTCCCTG , LRG_69:g.12124_12140delinsTCCAGCCCTTCTCCCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330377.3:c.*81_*97delinsTCCAGCCCTTCTCCCTG MANE Select	ENSP00000329312.2:n.*81_*97delinsTCCAGCCCTTCTCCCTG
ENST00000249053.3:c.*352_*368delinsTCCAGCCCTTCTCCCTG	ENSP00000249053.3:n.*352_*368delinsTCCAGCCCTTCTCCCTG
ENST00000330377.2:c.*81_*97delinsTCCAGCCCTTCTCCCTG	ENSP00000329312.2:n.*81_*97delinsTCCAGCCCTTCTCCCTG
NM_020070.3:c.*81_*97delinsTCCAGCCCTTCTCCCTG	NP_064455.1:n.*81_*97delinsTCCAGCCCTTCTCCCTG
NM_152855.2:c.*352_*368delinsTCCAGCCCTTCTCCCTG	NP_690594.1:n.*352_*368delinsTCCAGCCCTTCTCCCTG
XM_011530169.1:c.*81_*97delinsTCCAGCCCTTCTCCCTG	XP_011528471.1:n.*81_*97delinsTCCAGCCCTTCTCCCTG
XM_011530169.2:c.*81_*97delinsTCCAGCCCTTCTCCCTG	XP_011528471.1:n.*81_*97delinsTCCAGCCCTTCTCCCTG
NM_020070.4:c.*81_*97delinsTCCAGCCCTTCTCCCTG MANE Select	NP_064455.1:n.*81_*97delinsTCCAGCCCTTCTCCCTG
NM_001369906.1:c.*81_*97delinsTCCAGCCCTTCTCCCTG	NP_001356835.1:n.*81_*97delinsTCCAGCCCTTCTCCCTG
NM_152855.3:c.*352_*368delinsTCCAGCCCTTCTCCCTG	NP_690594.1:n.*352_*368delinsTCCAGCCCTTCTCCCTG