Canonical Allele Identifier: CA980962409

Gene: CXCL16

Linked Data

• dbSNP Id: rs1916094452
• gnomAD v3: 17-4734572-CCA-C
• gnomAD v4: 17-4734572-CCA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4734575_4734576del , CM000679.2:g.4734575_4734576del	GRCh38
NC_000017.10:g.4637870_4637871del , CM000679.1:g.4637870_4637871del	GRCh37
NC_000017.9:g.4584619_4584620del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293778.12:c.*23+9_*23+10del MANE Select	ENSP00000293778.7:n.*23+9_*23+10del
ENST00000574412.6:c.*32_*33del	ENSP00000459592.2:n.*32_*33del
ENST00000293778.10:c.*23+9_*23+10del	ENSP00000293778.6:n.*23+9_*23+10del
ENST00000574412.5:c.*32_*33del	ENSP00000459592.1:n.*32_*33del
ENST00000576153.5:n.579+9_579+10del
NM_001100812.1:c.*32_*33del	NP_001094282.1:n.*32_*33del
NM_022059.3:c.*23+9_*23+10del	NP_071342.2:n.*23+9_*23+10del
NM_022059.4:c.*23+9_*23+10del	NP_071342.2:n.*23+9_*23+10del
NM_001100812.2:c.*32_*33del	NP_001094282.2:n.*32_*33del
NM_001386809.1:c.*23+9_*23+10del MANE Select	NP_001373738.1:n.*23+9_*23+10del