Canonical Allele Identifier: CA980962148
Gene: CXCL16 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734380_4734381insATATG , CM000679.2:g.4734380_4734381insATATG GRCh38
NC_000017.10:g.4637675_4637676insATATG , CM000679.1:g.4637675_4637676insATATG GRCh37
NC_000017.9:g.4584424_4584425insATATG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293778.12:c.*124_*125insTATCA MANE Select ENSP00000293778.7:n.*124_*125insTATCA
ENST00000574412.6:c.*227_*228insTATCA ENSP00000459592.2:n.*227_*228insTATCA
ENST00000293778.10:c.*124_*125insTATCA ENSP00000293778.6:n.*124_*125insTATCA
ENST00000574412.5:c.*227_*228insTATCA ENSP00000459592.1:n.*227_*228insTATCA
ENST00000576153.5:n.680_681insTATCA
NM_022059.3:c.*124_*125insTATCA NP_071342.2:n.*124_*125insTATCA
NM_022059.4:c.*124_*125insTATCA NP_071342.2:n.*124_*125insTATCA
NM_001386809.1:c.*124_*125insTATCA MANE Select NP_001373738.1:n.*124_*125insTATCA