Canonical Allele Identifier: CA2190828056

Gene: IL16

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.81304249T>C , CM000677.2:g.81304249T>C	GRCh38
NC_000015.9:g.81596590T>C , CM000677.1:g.81596590T>C	GRCh37
NC_000015.8:g.79383645T>C	NCBI36
NG_029933.1:g.112372T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302987.10:c.3561+599T>C	ENSP00000302935.5:n.3561+599T>C
ENST00000706926.1:c.3420+599T>C	ENSP00000516648.1:n.3420+599T>C
ENST00000302987.9:c.3561+599T>C	ENSP00000302935.5:n.3561+599T>C
ENST00000683961.1:c.3420+599T>C MANE Select	ENSP00000508085.1:n.3420+599T>C
ENST00000302987.8:c.3420+599T>C	ENSP00000302935.4:n.3420+599T>C
ENST00000360547.9:c.*2597+599T>C	ENSP00000456972.1:n.*2597+599T>C
ENST00000394652.6:c.1317+599T>C	ENSP00000378147.2:n.1317+599T>C
ENST00000394660.6:c.3420+599T>C	ENSP00000378155.2:n.3420+599T>C
ENST00000558332.3:c.1331+599T>C
ENST00000558857.5:c.1534+599T>C	ENSP00000453131.1:n.1534+599T>C
ENST00000559342.1:n.264+599T>C
ENST00000559388.4:c.1317+599T>C	ENSP00000458125.2:n.1317+599T>C
ENST00000560115.5:c.3390+599T>C
NM_001172128.1:c.3420+599T>C	NP_001165599.1:n.3420+599T>C
NM_004513.5:c.1317+599T>C	NP_004504.3:n.1317+599T>C
NM_172217.3:c.3420+599T>C	NP_757366.2:n.3420+599T>C
XM_005254342.2:c.3561+599T>C	XP_005254399.1:n.3561+599T>C
XM_005254346.3:c.1317+599T>C	XP_005254403.1:n.1317+599T>C
XM_011521518.1:c.3282+599T>C	XP_011519820.1:n.3282+599T>C
XM_011521519.1:c.3420+599T>C	XP_011519821.1:n.3420+599T>C
XM_011521520.1:c.3420+599T>C	XP_011519822.1:n.3420+599T>C
XR_931805.1:n.3597+599T>C
NM_001352684.1:c.1590+599T>C	NP_001339613.1:n.1590+599T>C
NM_001352685.1:c.2910+599T>C	NP_001339614.1:n.2910+599T>C
NM_001352686.1:c.3573+599T>C	NP_001339615.1:n.3573+599T>C
NM_172217.4:c.3420+599T>C	NP_757366.2:n.3420+599T>C
NR_148035.1:n.3632+599T>C
NM_001172128.2:c.3420+599T>C	NP_001165599.1:n.3420+599T>C
NM_001352684.2:c.1590+599T>C	NP_001339613.1:n.1590+599T>C
NM_001352685.2:c.2910+599T>C	NP_001339614.1:n.2910+599T>C
NM_004513.6:c.1317+599T>C	NP_004504.3:n.1317+599T>C
NM_172217.5:c.3420+599T>C MANE Select	NP_757366.2:n.3420+599T>C
NR_148035.2:n.3631+599T>C
NM_001352686.2:c.3573+599T>C	NP_001339615.1:n.3573+599T>C