Canonical Allele Identifier: CA8309118
Gene: CXCL16 HGNC NCBI

Linked Data

dbSNP Id: rs754236501

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734615dup , CM000679.2:g.4734615dup GRCh38
NC_000017.10:g.4637910dup , CM000679.1:g.4637910dup GRCh37
NC_000017.9:g.4584659dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293778.12:c.756dup MANE Select ENSP00000293778.7:p.Asn253Ter
ENST00000574412.6:c.756dup ENSP00000459592.2:p.Asn253Ter
ENST00000293778.10:c.813dup ENSP00000293778.6:p.Asn272Ter
ENST00000574412.5:c.813dup ENSP00000459592.1:p.Asn272Ter
ENST00000575168.1:n.587dup
ENST00000576153.5:n.547dup
NM_001100812.1:c.813dup NP_001094282.1:p.Asn272Ter
NM_022059.3:c.813dup NP_071342.2:p.Asn272Ter
NM_022059.4:c.813dup NP_071342.2:p.Asn272Ter
NM_001100812.2:c.756dup NP_001094282.2:p.Asn253Ter
NM_001386809.1:c.756dup MANE Select NP_001373738.1:p.Asn253Ter