Canonical Allele Identifier: CA410898440
Community Standard Title: NM_020070.4(IGLL1):c.585G>C (p.Gln195His)
Gene: IGLL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.23573323C>G , CM000684.2:g.23573323C>G GRCh38
NC_000022.10:g.23915510C>G , CM000684.1:g.23915510C>G GRCh37
NC_000022.9:g.22245510C>G NCBI36
NG_009791.1:g.11986G>C , LRG_69:g.11986G>C

Transcript Alleles

HGVS Amino-acid Change
NM_020070.4:c.585G>C MANE Select NP_064455.1:p.Gln195His
ENST00000330377.3:c.585G>C MANE Select ENSP00000329312.2:p.Gln195His
NM_001369906.1:c.588G>C NP_001356835.1:p.Gln196His
NM_020070.3:c.585G>C NP_064455.1:p.Gln195His
NM_152855.2:c.*214G>C NP_690594.1:n.*214G>C
NM_152855.3:c.*214G>C NP_690594.1:n.*214G>C
ENST00000249053.3:c.*214G>C ENSP00000249053.3:n.*214G>C
ENST00000330377.2:c.585G>C ENSP00000329312.2:p.Gln195His
XM_011530169.1:c.588G>C XP_011528471.1:p.Gln196His
XM_011530169.2:c.588G>C XP_011528471.1:p.Gln196His