Canonical Allele Identifier: CA2190848292

Gene: IL16

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.81296675T= , CM000677.2:g.81296675T=	GRCh38
NC_000015.9:g.81589016T= , CM000677.1:g.81589016T=	GRCh37
NC_000015.8:g.79376071T=	NCBI36
NG_029933.1:g.104798T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000302987.10:c.2044-253T=	ENSP00000302935.5:n.2044-253T=
ENST00000706926.1:c.1903-253T=	ENSP00000516648.1:n.1903-253T=
ENST00000302987.9:c.2044-253T=	ENSP00000302935.5:n.2044-253T=
ENST00000683961.1:c.1903-253T= MANE Select	ENSP00000508085.1:n.1903-253T=
ENST00000302987.8:c.1903-253T=	ENSP00000302935.4:n.1903-253T=
ENST00000360547.9:c.*1080-253T=	ENSP00000456972.1:n.*1080-253T=
ENST00000394660.6:c.1903-253T=	ENSP00000378155.2:n.1903-253T=
ENST00000560115.5:c.1873-253T=
NM_001172128.1:c.1903-253T=	NP_001165599.1:n.1903-253T=
NM_172217.3:c.1903-253T=	NP_757366.2:n.1903-253T=
XM_005254342.2:c.2044-253T=	XP_005254399.1:n.2044-253T=
XM_005254346.3:c.-530T=	XP_005254403.1:n.-530T=
XM_011521518.1:c.1765-253T=	XP_011519820.1:n.1765-253T=
XM_011521519.1:c.1903-253T=	XP_011519821.1:n.1903-253T=
XM_011521520.1:c.1903-253T=	XP_011519822.1:n.1903-253T=
XR_931805.1:n.2004-253T=
NM_001352684.1:c.73-253T=	NP_001339613.1:n.73-253T=
NM_001352685.1:c.1393-253T=	NP_001339614.1:n.1393-253T=
NM_001352686.1:c.2056-253T=	NP_001339615.1:n.2056-253T=
NM_172217.4:c.1903-253T=	NP_757366.2:n.1903-253T=
NR_148035.1:n.2279-253T=
NM_001172128.2:c.1903-253T=	NP_001165599.1:n.1903-253T=
NM_001352684.2:c.73-253T=	NP_001339613.1:n.73-253T=
NM_001352685.2:c.1393-253T=	NP_001339614.1:n.1393-253T=
NM_172217.5:c.1903-253T= MANE Select	NP_757366.2:n.1903-253T=
NR_148035.2:n.2278-253T=
NM_001352686.2:c.2056-253T=	NP_001339615.1:n.2056-253T=