Canonical Allele Identifier: CA10143281
Gene: IGLL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.23573488A>G , CM000684.2:g.23573488A>G GRCh38
NC_000022.10:g.23915675A>G , CM000684.1:g.23915675A>G GRCh37
NC_000022.9:g.22245675A>G NCBI36
NG_009791.1:g.11821T>C , LRG_69:g.11821T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000330377.3:c.420T>C MANE Select ENSP00000329312.2:p.Phe140=
ENST00000249053.3:c.*49T>C ENSP00000249053.3:n.*49T>C
ENST00000330377.2:c.420T>C ENSP00000329312.2:p.Phe140=
ENST00000438703.1:c.423T>C ENSP00000403391.1:p.Phe141=
NM_020070.3:c.420T>C NP_064455.1:p.Phe140=
NM_152855.2:c.*49T>C NP_690594.1:n.*49T>C
XM_011530169.1:c.423T>C XP_011528471.1:p.Phe141=
XM_011530169.2:c.423T>C XP_011528471.1:p.Phe141=
NM_020070.4:c.420T>C MANE Select NP_064455.1:p.Phe140=
NM_001369906.1:c.423T>C NP_001356835.1:p.Phe141=
NM_152855.3:c.*49T>C NP_690594.1:n.*49T>C