Canonical Allele Identifier: CA2244538520
Gene: CXCL16 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4738774A>T , CM000679.2:g.4738774A>T GRCh38
NC_000017.10:g.4642069A>T , CM000679.1:g.4642069A>T GRCh37
NC_000017.9:g.4588818A>T NCBI36
NG_034160.1:g.3760A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000293778.12:c.218+8T>A MANE Select ENSP00000293778.7:n.218+8T>A
ENST00000574412.6:c.218+8T>A ENSP00000459592.2:n.218+8T>A
ENST00000293778.10:c.275+8T>A ENSP00000293778.6:n.275+8T>A
ENST00000573123.1:c.56+8T>A ENSP00000460145.1:n.56+8T>A
ENST00000574412.5:c.275+8T>A ENSP00000459592.1:n.275+8T>A
NM_001100812.1:c.275+8T>A NP_001094282.1:n.275+8T>A
NM_022059.3:c.275+8T>A NP_071342.2:n.275+8T>A
NM_022059.4:c.275+8T>A NP_071342.2:n.275+8T>A
NM_001100812.2:c.218+8T>A NP_001094282.2:n.218+8T>A
NM_001386809.1:c.218+8T>A MANE Select NP_001373738.1:n.218+8T>A