Canonical Allele Identifier: CA2397855929
Gene: IGLL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.23573454C= , CM000684.2:g.23573454C= GRCh38
NC_000022.10:g.23915641C= , CM000684.1:g.23915641C= GRCh37
NC_000022.9:g.22245641C= NCBI36
NG_009791.1:g.11855G= , LRG_69:g.11855G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000330377.3:c.454G= MANE Select ENSP00000329312.2:p.Asp152=
ENST00000249053.3:c.*83G= ENSP00000249053.3:n.*83G=
ENST00000330377.2:c.454G= ENSP00000329312.2:p.Asp152=
ENST00000438703.1:c.457G= ENSP00000403391.1:p.Asp153=
NM_020070.3:c.454G= NP_064455.1:p.Asp152=
NM_152855.2:c.*83G= NP_690594.1:n.*83G=
XM_011530169.1:c.457G= XP_011528471.1:p.Asp153=
XM_011530169.2:c.457G= XP_011528471.1:p.Asp153=
NM_020070.4:c.454G= MANE Select NP_064455.1:p.Asp152=
NM_001369906.1:c.457G= NP_001356835.1:p.Asp153=
NM_152855.3:c.*83G= NP_690594.1:n.*83G=