Canonical Allele Identifier: CA2190848368

Gene: IL16

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.81296740G= , CM000677.2:g.81296740G=	GRCh38
NC_000015.9:g.81589081G= , CM000677.1:g.81589081G=	GRCh37
NC_000015.8:g.79376136G=	NCBI36
NG_029933.1:g.104863G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302987.10:c.2044-188G=	ENSP00000302935.5:n.2044-188G=
ENST00000706926.1:c.1903-188G=	ENSP00000516648.1:n.1903-188G=
ENST00000302987.9:c.2044-188G=	ENSP00000302935.5:n.2044-188G=
ENST00000683961.1:c.1903-188G= MANE Select	ENSP00000508085.1:n.1903-188G=
ENST00000302987.8:c.1903-188G=	ENSP00000302935.4:n.1903-188G=
ENST00000360547.9:c.*1080-188G=	ENSP00000456972.1:n.*1080-188G=
ENST00000394660.6:c.1903-188G=	ENSP00000378155.2:n.1903-188G=
ENST00000560115.5:c.1873-188G=
NM_001172128.1:c.1903-188G=	NP_001165599.1:n.1903-188G=
NM_172217.3:c.1903-188G=	NP_757366.2:n.1903-188G=
XM_005254342.2:c.2044-188G=	XP_005254399.1:n.2044-188G=
XM_005254346.3:c.-465G=	XP_005254403.1:n.-465G=
XM_011521518.1:c.1765-188G=	XP_011519820.1:n.1765-188G=
XM_011521519.1:c.1903-188G=	XP_011519821.1:n.1903-188G=
XM_011521520.1:c.1903-188G=	XP_011519822.1:n.1903-188G=
XR_931805.1:n.2004-188G=
NM_001352684.1:c.73-188G=	NP_001339613.1:n.73-188G=
NM_001352685.1:c.1393-188G=	NP_001339614.1:n.1393-188G=
NM_001352686.1:c.2056-188G=	NP_001339615.1:n.2056-188G=
NM_172217.4:c.1903-188G=	NP_757366.2:n.1903-188G=
NR_148035.1:n.2279-188G=
NM_001172128.2:c.1903-188G=	NP_001165599.1:n.1903-188G=
NM_001352684.2:c.73-188G=	NP_001339613.1:n.73-188G=
NM_001352685.2:c.1393-188G=	NP_001339614.1:n.1393-188G=
NM_172217.5:c.1903-188G= MANE Select	NP_757366.2:n.1903-188G=
NR_148035.2:n.2278-188G=
NM_001352686.2:c.2056-188G=	NP_001339615.1:n.2056-188G=