Canonical Allele Identifier: CA2190855784

Gene: IL16

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.81300461A= , CM000677.2:g.81300461A=	GRCh38
NC_000015.9:g.81592802A= , CM000677.1:g.81592802A=	GRCh37
NC_000015.8:g.79379857A=	NCBI36
NG_029933.1:g.108584A=

Transcript Alleles

HGVS	Amino-acid Change
NM_172217.5:c.3135A= MANE Select	NP_757366.2:p.Thr1045=
ENST00000683961.1:c.3135A= MANE Select	ENSP00000508085.1:p.Thr1045=
NM_001172128.1:c.3135A=	NP_001165599.1:p.Thr1045=
NM_001172128.2:c.3135A=	NP_001165599.1:p.Thr1045=
NM_001352684.1:c.1305A=	NP_001339613.1:p.Thr435=
NM_001352684.2:c.1305A=	NP_001339613.1:p.Thr435=
NM_001352685.1:c.2625A=	NP_001339614.1:p.Thr875=
NM_001352685.2:c.2625A=	NP_001339614.1:p.Thr875=
NM_001352686.1:c.3288A=	NP_001339615.1:p.Thr1096=
NM_001352686.2:c.3288A=	NP_001339615.1:p.Thr1096=
NM_004513.5:c.1032A=	NP_004504.3:p.Thr344=
NM_004513.6:c.1032A=	NP_004504.3:p.Thr344=
NM_172217.3:c.3135A=	NP_757366.2:p.Thr1045=
NM_172217.4:c.3135A=	NP_757366.2:p.Thr1045=
NR_148035.1:n.3347A=
NR_148035.2:n.3346A=
ENST00000302987.10:c.3276A=	ENSP00000302935.5:p.Thr1092=
ENST00000302987.8:c.3135A=	ENSP00000302935.4:p.Thr1045=
ENST00000302987.9:c.3276A=	ENSP00000302935.5:p.Thr1092=
ENST00000360547.9:c.*2312A=	ENSP00000456972.1:n.*2312A=
ENST00000394652.6:c.1032A=	ENSP00000378147.2:p.Thr344=
ENST00000394660.6:c.3135A=	ENSP00000378155.2:p.Thr1045=
ENST00000558332.3:c.1046A=
ENST00000558857.5:c.1249A=	ENSP00000453131.1:n.1249A=
ENST00000559388.4:c.1032A=	ENSP00000458125.2:p.Thr344=
ENST00000560115.5:c.3105A=
ENST00000706926.1:c.3135A=	ENSP00000516648.1:p.Thr1045=
XM_005254342.2:c.3276A=	XP_005254399.1:p.Thr1092=
XM_005254346.3:c.1032A=	XP_005254403.1:p.Thr344=
XM_011521518.1:c.2997A=	XP_011519820.1:p.Thr999=
XM_011521519.1:c.3135A=	XP_011519821.1:p.Thr1045=
XM_011521520.1:c.3135A=	XP_011519822.1:p.Thr1045=
XR_931805.1:n.3312A=