Canonical Allele Identifier: CA513685858
Community Standard Title: NM_020070.4(IGLL1):c.444C>G (p.Thr148=)
Gene: IGLL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.23573464G>C , CM000684.2:g.23573464G>C GRCh38
NC_000022.10:g.23915651G>C , CM000684.1:g.23915651G>C GRCh37
NC_000022.9:g.22245651G>C NCBI36
NG_009791.1:g.11845C>G , LRG_69:g.11845C>G

Transcript Alleles

HGVS Amino-acid Change
NM_020070.4:c.444C>G MANE Select NP_064455.1:p.Thr148=
ENST00000330377.3:c.444C>G MANE Select ENSP00000329312.2:p.Thr148=
NM_001369906.1:c.447C>G NP_001356835.1:p.Thr149=
NM_020070.3:c.444C>G NP_064455.1:p.Thr148=
NM_152855.2:c.*73C>G NP_690594.1:n.*73C>G
NM_152855.3:c.*73C>G NP_690594.1:n.*73C>G
ENST00000249053.3:c.*73C>G ENSP00000249053.3:n.*73C>G
ENST00000330377.2:c.444C>G ENSP00000329312.2:p.Thr148=
ENST00000438703.1:c.447C>G ENSP00000403391.1:p.Thr149=
XM_011530169.1:c.447C>G XP_011528471.1:p.Thr149=
XM_011530169.2:c.447C>G XP_011528471.1:p.Thr149=