Canonical Allele Identifier: CA2397855800
Gene: IGLL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.23573251G= , CM000684.2:g.23573251G= GRCh38
NC_000022.10:g.23915438G= , CM000684.1:g.23915438G= GRCh37
NC_000022.9:g.22245438G= NCBI36
NG_009791.1:g.12058C= , LRG_69:g.12058C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000330377.3:c.*15C= MANE Select ENSP00000329312.2:n.*15C=
ENST00000249053.3:c.*286C= ENSP00000249053.3:n.*286C=
ENST00000330377.2:c.*15C= ENSP00000329312.2:n.*15C=
NM_020070.3:c.*15C= NP_064455.1:n.*15C=
NM_152855.2:c.*286C= NP_690594.1:n.*286C=
XM_011530169.1:c.*15C= XP_011528471.1:n.*15C=
XM_011530169.2:c.*15C= XP_011528471.1:n.*15C=
NM_020070.4:c.*15C= MANE Select NP_064455.1:n.*15C=
NM_001369906.1:c.*15C= NP_001356835.1:n.*15C=
NM_152855.3:c.*286C= NP_690594.1:n.*286C=