Canonical Allele Identifier: CA2190811890

Gene: IL16

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.81206630T= , CM000677.2:g.81206630T=	GRCh38
NC_000015.9:g.81498971T= , CM000677.1:g.81498971T=	GRCh37
NC_000015.8:g.79286026T=	NCBI36
NG_029933.1:g.14753T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302987.10:c.41-18669T=	ENSP00000302935.5:n.41-18669T=
ENST00000706926.1:c.-102+6768T=	ENSP00000516648.1:n.-102+6768T=
ENST00000302987.9:c.41-18669T=	ENSP00000302935.5:n.41-18669T=
ENST00000683961.1:c.-102+9478T= MANE Select	ENSP00000508085.1:n.-102+9478T=
ENST00000360547.9:c.-102+18227T=	ENSP00000456972.1:n.-102+18227T=
ENST00000394660.6:c.-102+9493T=	ENSP00000378155.2:n.-102+9493T=
ENST00000559383.5:c.-102+9478T=	ENSP00000453250.1:n.-102+9478T=
ENST00000560241.5:c.-101-18669T=	ENSP00000452738.1:n.-101-18669T=
NM_001172128.1:c.-102+9493T=	NP_001165599.1:n.-102+9493T=
XM_005254342.2:c.41-18669T=	XP_005254399.1:n.41-18669T=
XM_011521520.1:c.-102+9478T=	XP_011519822.1:n.-102+9478T=
NM_001352684.1:c.-2121+9478T=	NP_001339613.1:n.-2121+9478T=
NM_001352685.1:c.-760+9478T=	NP_001339614.1:n.-760+9478T=
NM_001352686.1:c.52+6768T=	NP_001339615.1:n.52+6768T=
NM_172217.4:c.-102+9478T=	NP_757366.2:n.-102+9478T=
NR_148035.1:n.275+9478T=
NM_001172128.2:c.-102+9493T=	NP_001165599.1:n.-102+9493T=
NM_001352684.2:c.-2121+9478T=	NP_001339613.1:n.-2121+9478T=
NM_001352685.2:c.-760+9478T=	NP_001339614.1:n.-760+9478T=
NM_172217.5:c.-102+9478T= MANE Select	NP_757366.2:n.-102+9478T=
NR_148035.2:n.274+9478T=
NM_001352686.2:c.52+6768T=	NP_001339615.1:n.52+6768T=