Canonical Allele Identifier: CA2635550248
Gene: CXCL16 HGNC NCBI

Linked Data

gnomAD v4: 17-4734517-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734517G>A , CM000679.2:g.4734517G>A GRCh38
NC_000017.10:g.4637812G>A , CM000679.1:g.4637812G>A GRCh37
NC_000017.9:g.4584561G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293778.12:c.*24-38C>T MANE Select ENSP00000293778.7:n.*24-38C>T
ENST00000574412.6:c.*89C>T ENSP00000459592.2:n.*89C>T
ENST00000293778.10:c.*24-38C>T ENSP00000293778.6:n.*24-38C>T
ENST00000574412.5:c.*89C>T ENSP00000459592.1:n.*89C>T
ENST00000576153.5:n.580-38C>T
NM_001100812.1:c.*89C>T NP_001094282.1:n.*89C>T
NM_022059.3:c.*24-38C>T NP_071342.2:n.*24-38C>T
NM_022059.4:c.*24-38C>T NP_071342.2:n.*24-38C>T
NM_001100812.2:c.*89C>T NP_001094282.2:n.*89C>T
NM_001386809.1:c.*24-38C>T MANE Select NP_001373738.1:n.*24-38C>T