Canonical Allele Identifier: CA2397855802
Gene: IGLL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.23573253C= , CM000684.2:g.23573253C= GRCh38
NC_000022.10:g.23915440C= , CM000684.1:g.23915440C= GRCh37
NC_000022.9:g.22245440C= NCBI36
NG_009791.1:g.12056G= , LRG_69:g.12056G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000330377.3:c.*13G= MANE Select ENSP00000329312.2:n.*13G=
ENST00000249053.3:c.*284G= ENSP00000249053.3:n.*284G=
ENST00000330377.2:c.*13G= ENSP00000329312.2:n.*13G=
NM_020070.3:c.*13G= NP_064455.1:n.*13G=
NM_152855.2:c.*284G= NP_690594.1:n.*284G=
XM_011530169.1:c.*13G= XP_011528471.1:n.*13G=
XM_011530169.2:c.*13G= XP_011528471.1:n.*13G=
NM_020070.4:c.*13G= MANE Select NP_064455.1:n.*13G=
NM_001369906.1:c.*13G= NP_001356835.1:n.*13G=
NM_152855.3:c.*284G= NP_690594.1:n.*284G=