Canonical Allele Identifier: CA393271181

Gene: IL16

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.81285798C>A , CM000677.2:g.81285798C>A	GRCh38
NC_000015.9:g.81578139C>A , CM000677.1:g.81578139C>A	GRCh37
NC_000015.8:g.79365194C>A	NCBI36
NG_029933.1:g.93921C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302987.10:c.1441C>A	ENSP00000302935.5:p.Pro481Thr
ENST00000706926.1:c.1300C>A	ENSP00000516648.1:p.Pro434Thr
ENST00000302987.9:c.1441C>A	ENSP00000302935.5:p.Pro481Thr
ENST00000683961.1:c.1300C>A MANE Select	ENSP00000508085.1:p.Pro434Thr
ENST00000302987.8:c.1300C>A	ENSP00000302935.4:p.Pro434Thr
ENST00000360547.9:c.1300C>A	ENSP00000456972.1:p.Pro434Thr
ENST00000394660.6:c.1300C>A	ENSP00000378155.2:p.Pro434Thr
ENST00000559383.5:c.1300C>A	ENSP00000453250.1:p.Pro434Thr
ENST00000560115.5:c.449C>A
ENST00000560241.5:c.1300C>A	ENSP00000452738.1:p.Pro434Thr
NM_001172128.1:c.1300C>A	NP_001165599.1:p.Pro434Thr
NM_172217.3:c.1300C>A	NP_757366.2:p.Pro434Thr
XM_005254342.2:c.1441C>A	XP_005254399.1:p.Pro481Thr
XM_011521518.1:c.1300C>A	XP_011519820.1:p.Pro434Thr
XM_011521519.1:c.1300C>A	XP_011519821.1:p.Pro434Thr
XM_011521520.1:c.1300C>A	XP_011519822.1:p.Pro434Thr
XR_931805.1:n.1401C>A
NM_001352684.1:c.-720C>A	NP_001339613.1:n.-720C>A
NM_001352685.1:c.790C>A	NP_001339614.1:p.Pro264Thr
NM_001352686.1:c.1453C>A	NP_001339615.1:p.Pro485Thr
NM_172217.4:c.1300C>A	NP_757366.2:p.Pro434Thr
NR_148035.1:n.1676C>A
NM_001172128.2:c.1300C>A	NP_001165599.1:p.Pro434Thr
NM_001352684.2:c.-720C>A	NP_001339613.1:n.-720C>A
NM_001352685.2:c.790C>A	NP_001339614.1:p.Pro264Thr
NM_172217.5:c.1300C>A MANE Select	NP_757366.2:p.Pro434Thr
NR_148035.2:n.1675C>A
NM_001352686.2:c.1453C>A	NP_001339615.1:p.Pro485Thr