Canonical Allele Identifier: CA2190829844

Gene: IL16

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.81305928T= , CM000677.2:g.81305928T=	GRCh38
NC_000015.9:g.81598269T= , CM000677.1:g.81598269T=	GRCh37
NC_000015.8:g.79385324T=	NCBI36
NG_029933.1:g.114051T=

Transcript Alleles

HGVS	Amino-acid Change
NM_172217.5:c.3441T= MANE Select	NP_757366.2:p.Asn1147=
ENST00000683961.1:c.3441T= MANE Select	ENSP00000508085.1:p.Asn1147=
NM_001172128.1:c.3441T=	NP_001165599.1:p.Asn1147=
NM_001172128.2:c.3441T=	NP_001165599.1:p.Asn1147=
NM_001352684.1:c.1611T=	NP_001339613.1:p.Asn537=
NM_001352684.2:c.1611T=	NP_001339613.1:p.Asn537=
NM_001352685.1:c.2931T=	NP_001339614.1:p.Asn977=
NM_001352685.2:c.2931T=	NP_001339614.1:p.Asn977=
NM_001352686.1:c.3594T=	NP_001339615.1:p.Asn1198=
NM_001352686.2:c.3594T=	NP_001339615.1:p.Asn1198=
NM_004513.5:c.1338T=	NP_004504.3:p.Asn446=
NM_004513.6:c.1338T=	NP_004504.3:p.Asn446=
NM_172217.3:c.3441T=	NP_757366.2:p.Asn1147=
NM_172217.4:c.3441T=	NP_757366.2:p.Asn1147=
NR_148035.1:n.3653T=
NR_148035.2:n.3652T=
ENST00000302987.10:c.3582T=	ENSP00000302935.5:p.Asn1194=
ENST00000302987.8:c.3441T=	ENSP00000302935.4:p.Asn1147=
ENST00000302987.9:c.3582T=	ENSP00000302935.5:p.Asn1194=
ENST00000360547.9:c.*2618T=	ENSP00000456972.1:n.*2618T=
ENST00000394652.6:c.1338T=	ENSP00000378147.2:p.Asn446=
ENST00000394660.6:c.3441T=	ENSP00000378155.2:p.Asn1147=
ENST00000558332.3:c.1352T=
ENST00000558857.5:c.1555T=	ENSP00000453131.1:n.1555T=
ENST00000559342.1:n.285T=
ENST00000559388.4:c.1338T=	ENSP00000458125.2:p.Asn446=
ENST00000559953.1:n.183T=
ENST00000560115.5:c.3411T=
ENST00000706926.1:c.3441T=	ENSP00000516648.1:p.Asn1147=
XM_005254342.2:c.3582T=	XP_005254399.1:p.Asn1194=
XM_005254346.3:c.1338T=	XP_005254403.1:p.Asn446=
XM_011521518.1:c.3303T=	XP_011519820.1:p.Asn1101=
XM_011521519.1:c.3441T=	XP_011519821.1:p.Asn1147=
XM_011521520.1:c.3441T=	XP_011519822.1:p.Asn1147=
XR_931805.1:n.3618T=