Canonical Allele Identifier: CA14136743

Gene: IL16

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.81266282T>C , CM000677.2:g.81266282T>C	GRCh38
NC_000015.9:g.81558623T>C , CM000677.1:g.81558623T>C	GRCh37
NC_000015.8:g.79345678T>C	NCBI36
NG_029933.1:g.74405T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302987.10:c.705+481T>C	ENSP00000302935.5:n.705+481T>C
ENST00000706926.1:c.564+481T>C	ENSP00000516648.1:n.564+481T>C
ENST00000302987.9:c.705+481T>C	ENSP00000302935.5:n.705+481T>C
ENST00000683961.1:c.564+481T>C MANE Select	ENSP00000508085.1:n.564+481T>C
ENST00000302987.8:c.564+481T>C	ENSP00000302935.4:n.564+481T>C
ENST00000360547.9:c.564+481T>C	ENSP00000456972.1:n.564+481T>C
ENST00000394660.6:c.564+481T>C	ENSP00000378155.2:n.564+481T>C
ENST00000559383.5:c.564+481T>C	ENSP00000453250.1:n.564+481T>C
ENST00000560241.5:c.564+481T>C	ENSP00000452738.1:n.564+481T>C
NM_001172128.1:c.564+481T>C	NP_001165599.1:n.564+481T>C
NM_172217.3:c.564+481T>C	NP_757366.2:n.564+481T>C
XM_005254342.2:c.705+481T>C	XP_005254399.1:n.705+481T>C
XM_011521518.1:c.564+481T>C	XP_011519820.1:n.564+481T>C
XM_011521519.1:c.564+481T>C	XP_011519821.1:n.564+481T>C
XM_011521520.1:c.564+481T>C	XP_011519822.1:n.564+481T>C
XR_931805.1:n.665+481T>C
NM_001352684.1:c.-1456+481T>C	NP_001339613.1:n.-1456+481T>C
NM_001352685.1:c.-94-372T>C	NP_001339614.1:n.-94-372T>C
NM_001352686.1:c.717+481T>C	NP_001339615.1:n.717+481T>C
NM_172217.4:c.564+481T>C	NP_757366.2:n.564+481T>C
NR_148035.1:n.940+481T>C
NM_001172128.2:c.564+481T>C	NP_001165599.1:n.564+481T>C
NM_001352684.2:c.-1456+481T>C	NP_001339613.1:n.-1456+481T>C
NM_001352685.2:c.-94-372T>C	NP_001339614.1:n.-94-372T>C
NM_172217.5:c.564+481T>C MANE Select	NP_757366.2:n.564+481T>C
NR_148035.2:n.939+481T>C
NM_001352686.2:c.717+481T>C	NP_001339615.1:n.717+481T>C