Canonical Allele Identifier: CA2190830113

Gene: IL16

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.81306075G= , CM000677.2:g.81306075G=	GRCh38
NC_000015.9:g.81598416G= , CM000677.1:g.81598416G=	GRCh37
NC_000015.8:g.79385471G=	NCBI36
NG_029933.1:g.114198G=

Transcript Alleles

HGVS	Amino-acid Change
NM_172217.5:c.3588G= MANE Select	NP_757366.2:p.Arg1196=
ENST00000683961.1:c.3588G= MANE Select	ENSP00000508085.1:p.Arg1196=
NM_001172128.1:c.3588G=	NP_001165599.1:p.Arg1196=
NM_001172128.2:c.3588G=	NP_001165599.1:p.Arg1196=
NM_001352684.1:c.1758G=	NP_001339613.1:p.Arg586=
NM_001352684.2:c.1758G=	NP_001339613.1:p.Arg586=
NM_001352685.1:c.3078G=	NP_001339614.1:p.Arg1026=
NM_001352685.2:c.3078G=	NP_001339614.1:p.Arg1026=
NM_001352686.1:c.3741G=	NP_001339615.1:p.Arg1247=
NM_001352686.2:c.3741G=	NP_001339615.1:p.Arg1247=
NM_004513.5:c.1485G=	NP_004504.3:p.Arg495=
NM_004513.6:c.1485G=	NP_004504.3:p.Arg495=
NM_172217.3:c.3588G=	NP_757366.2:p.Arg1196=
NM_172217.4:c.3588G=	NP_757366.2:p.Arg1196=
NR_148035.1:n.3800G=
NR_148035.2:n.3799G=
ENST00000302987.10:c.3729G=	ENSP00000302935.5:p.Arg1243=
ENST00000302987.8:c.3588G=	ENSP00000302935.4:p.Arg1196=
ENST00000302987.9:c.3729G=	ENSP00000302935.5:p.Arg1243=
ENST00000360547.9:c.*2765G=	ENSP00000456972.1:n.*2765G=
ENST00000394652.6:c.1485G=	ENSP00000378147.2:p.Arg495=
ENST00000394660.6:c.3588G=	ENSP00000378155.2:p.Arg1196=
ENST00000558332.3:c.1499G=
ENST00000558857.5:c.1702G=	ENSP00000453131.1:n.1702G=
ENST00000559342.1:n.432G=
ENST00000559388.4:c.1485G=	ENSP00000458125.2:p.Arg495=
ENST00000559953.1:n.330G=
ENST00000560115.5:c.3558G=
ENST00000706926.1:c.3588G=	ENSP00000516648.1:p.Arg1196=
XM_005254342.2:c.3729G=	XP_005254399.1:p.Arg1243=
XM_005254346.3:c.1485G=	XP_005254403.1:p.Arg495=
XM_011521518.1:c.3450G=	XP_011519820.1:p.Arg1150=
XM_011521519.1:c.3588G=	XP_011519821.1:p.Arg1196=
XM_011521520.1:c.3588G=	XP_011519822.1:p.Arg1196=
XR_931805.1:n.3765G=