Canonical Allele Identifier: CA397281549

Gene: CXCL16

Linked Data

• gnomAD v4: 17-4734638-A-C
• MyVariant Identifiers: chr17:g.4637933A>C (hg19) ; chr17:g.4734638A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4734638A>C , CM000679.2:g.4734638A>C	GRCh38
NC_000017.10:g.4637933A>C , CM000679.1:g.4637933A>C	GRCh37
NC_000017.9:g.4584682A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293778.12:c.733T>G MANE Select	ENSP00000293778.7:p.Tyr245Asp
ENST00000574412.6:c.733T>G	ENSP00000459592.2:p.Tyr245Asp
ENST00000293778.10:c.790T>G	ENSP00000293778.6:p.Tyr264Asp
ENST00000574412.5:c.790T>G	ENSP00000459592.1:p.Tyr264Asp
ENST00000575168.1:n.564T>G
ENST00000576153.5:n.524T>G
NM_001100812.1:c.790T>G	NP_001094282.1:p.Tyr264Asp
NM_022059.3:c.790T>G	NP_071342.2:p.Tyr264Asp
NM_022059.4:c.790T>G	NP_071342.2:p.Tyr264Asp
NM_001100812.2:c.733T>G	NP_001094282.2:p.Tyr245Asp
NM_001386809.1:c.733T>G MANE Select	NP_001373738.1:p.Tyr245Asp