Canonical Allele Identifier: CA1024476080
Gene: IGLL1 HGNC NCBI

Linked Data

dbSNP Id: rs1924854683

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.23573167T>C , CM000684.2:g.23573167T>C GRCh38
NC_000022.10:g.23915354T>C , CM000684.1:g.23915354T>C GRCh37
NC_000022.9:g.22245354T>C NCBI36
NG_009791.1:g.12142A>G , LRG_69:g.12142A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000330377.3:c.*99A>G MANE Select ENSP00000329312.2:n.*99A>G
ENST00000249053.3:c.*370A>G ENSP00000249053.3:n.*370A>G
ENST00000330377.2:c.*99A>G ENSP00000329312.2:n.*99A>G
NM_020070.3:c.*99A>G NP_064455.1:n.*99A>G
NM_152855.2:c.*370A>G NP_690594.1:n.*370A>G
XM_011530169.1:c.*99A>G XP_011528471.1:n.*99A>G
XM_011530169.2:c.*99A>G XP_011528471.1:n.*99A>G
NM_020070.4:c.*99A>G MANE Select NP_064455.1:n.*99A>G
NM_001369906.1:c.*99A>G NP_001356835.1:n.*99A>G
NM_152855.3:c.*370A>G NP_690594.1:n.*370A>G