Canonical Allele Identifier: CA2190834225

Gene: IL16

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.81308981A= , CM000677.2:g.81308981A=	GRCh38
NC_000015.9:g.81601322A= , CM000677.1:g.81601322A=	GRCh37
NC_000015.8:g.79388377A=	NCBI36
NG_029933.1:g.117104A=

Transcript Alleles

HGVS	Amino-acid Change
NM_172217.5:c.*183A= MANE Select	NP_757366.2:n.*183A=
ENST00000683961.1:c.*183A= MANE Select	ENSP00000508085.1:n.*183A=
NM_001172128.1:c.*183A=	NP_001165599.1:n.*183A=
NM_001172128.2:c.*183A=	NP_001165599.1:n.*183A=
NM_001352684.1:c.*183A=	NP_001339613.1:n.*183A=
NM_001352684.2:c.*183A=	NP_001339613.1:n.*183A=
NM_001352685.1:c.*183A=	NP_001339614.1:n.*183A=
NM_001352685.2:c.*183A=	NP_001339614.1:n.*183A=
NM_001352686.1:c.*183A=	NP_001339615.1:n.*183A=
NM_001352686.2:c.*183A=	NP_001339615.1:n.*183A=
NM_004513.5:c.*183A=	NP_004504.3:n.*183A=
NM_004513.6:c.*183A=	NP_004504.3:n.*183A=
NM_172217.3:c.*183A=	NP_757366.2:n.*183A=
NM_172217.4:c.*183A=	NP_757366.2:n.*183A=
NR_148035.1:n.4394A=
NR_148035.2:n.4393A=
ENST00000302987.10:c.*183A=	ENSP00000302935.5:n.*183A=
ENST00000302987.9:c.*183A=	ENSP00000302935.5:n.*183A=
ENST00000360547.9:c.*3359A=	ENSP00000456972.1:n.*3359A=
ENST00000394652.6:c.*183A=	ENSP00000378147.2:n.*183A=
ENST00000394660.6:c.*183A=	ENSP00000378155.2:n.*183A=
ENST00000706926.1:c.*183A=	ENSP00000516648.1:n.*183A=
XM_005254342.2:c.*183A=	XP_005254399.1:n.*183A=
XM_005254346.3:c.*183A=	XP_005254403.1:n.*183A=
XM_011521518.1:c.*183A=	XP_011519820.1:n.*183A=
XM_011521520.1:c.*183A=	XP_011519822.1:n.*183A=