Canonical Allele Identifier: CA980962158

Gene: CXCL16

Linked Data

• gnomAD v3: 17-4734382-T-TTTGCCTGTGTCCCCACCCAAATCTCATCTTGAATTCTCACGTGTTGTGGGA
• gnomAD v4: 17-4734382-T-TTTGCCTGTGTCCCCACCCAAATCTCATCTTGAATTCTCACGTGTTGTGGGA

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4734382_4734383insTTGCCTGTGTCCCCACCCAAATCTCATCTTGAATTCTCACGTGTTGTGGGA , CM000679.2:g.4734382_4734383insTTGCCTGTGTCCCCACCCAAATCTCATCTTGAATTCTCACGTGTTGTGGGA	GRCh38
NC_000017.10:g.4637677_4637678insTTGCCTGTGTCCCCACCCAAATCTCATCTTGAATTCTCACGTGTTGTGGGA , CM000679.1:g.4637677_4637678insTTGCCTGTGTCCCCACCCAAATCTCATCTTGAATTCTCACGTGTTGTGGGA	GRCh37
NC_000017.9:g.4584426_4584427insTTGCCTGTGTCCCCACCCAAATCTCATCTTGAATTCTCACGTGTTGTGGGA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293778.12:c.*120_*121insTCCCACAACACGTGAGAATTCAAGATGAGATTTGGGTGGGGACACAGGCAA MANE Select	ENSP00000293778.7:n.*120_*121insTCCCACAACACGTGAGAATTCAAGATGAG...
ENST00000574412.6:c.*223_*224insTCCCACAACACGTGAGAATTCAAGATGAGATTTGGGTGGGGACACAGGCAA	ENSP00000459592.2:n.*223_*224insTCCCACAACACGTGAGAATTCAAGATGAG...
ENST00000293778.10:c.*120_*121insTCCCACAACACGTGAGAATTCAAGATGAGATTTGGGTGGGGACACAGGCAA	ENSP00000293778.6:n.*120_*121insTCCCACAACACGTGAGAATTCAAGATGAG...
ENST00000574412.5:c.*223_*224insTCCCACAACACGTGAGAATTCAAGATGAGATTTGGGTGGGGACACAGGCAA	ENSP00000459592.1:n.*223_*224insTCCCACAACACGTGAGAATTCAAGATGAG...
ENST00000576153.5:n.676_677insTCCCACAACACGTGAGAATTCAAGATGAGATTTGGGTGGGGACACAGGCAA
NM_022059.3:c.*120_*121insTCCCACAACACGTGAGAATTCAAGATGAGATTTGGGTGGGGACACAGGCAA	NP_071342.2:n.*120_*121insTCCCACAACACGTGAGAATTCAAGATGAGATTTGG...
NM_022059.4:c.*120_*121insTCCCACAACACGTGAGAATTCAAGATGAGATTTGGGTGGGGACACAGGCAA	NP_071342.2:n.*120_*121insTCCCACAACACGTGAGAATTCAAGATGAGATTTGG...
NM_001386809.1:c.*120_*121insTCCCACAACACGTGAGAATTCAAGATGAGATTTGGGTGGGGACACAGGCAA MANE Select	NP_001373738.1:n.*120_*121insTCCCACAACACGTGAGAATTCAAGATGAGATT...