Canonical Allele Identifier: CA2397855888
Gene: IGLL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.23573391A= , CM000684.2:g.23573391A= GRCh38
NC_000022.10:g.23915578A= , CM000684.1:g.23915578A= GRCh37
NC_000022.9:g.22245578A= NCBI36
NG_009791.1:g.11918T= , LRG_69:g.11918T=

Transcript Alleles

HGVS Amino-acid change
ENST00000330377.3:c.517T= MANE Select ENSP00000329312.2:p.Tyr173=
ENST00000249053.3:c.*146T= ENSP00000249053.3:n.*146T=
ENST00000330377.2:c.517T= ENSP00000329312.2:p.Tyr173=
ENST00000438703.1:c.520T= ENSP00000403391.1:p.Tyr174=
NM_020070.3:c.517T= NP_064455.1:p.Tyr173=
NM_152855.2:c.*146T= NP_690594.1:n.*146T=
XM_011530169.1:c.520T= XP_011528471.1:p.Tyr174=
XM_011530169.2:c.520T= XP_011528471.1:p.Tyr174=
NM_020070.4:c.517T= MANE Select NP_064455.1:p.Tyr173=
NM_001369906.1:c.520T= NP_001356835.1:p.Tyr174=
NM_152855.3:c.*146T= NP_690594.1:n.*146T=