Canonical Allele Identifier: CA2190810722

Gene: IL16

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.81241354C= , CM000677.2:g.81241354C=	GRCh38
NC_000015.9:g.81533695C= , CM000677.1:g.81533695C=	GRCh37
NC_000015.8:g.79320750C=	NCBI36
NG_029933.1:g.49477C=

Transcript Alleles

HGVS	Amino-acid Change
NM_172217.5:c.312+15643C= MANE Select	NP_757366.2:n.312+15643C=
ENST00000683961.1:c.312+15643C= MANE Select	ENSP00000508085.1:n.312+15643C=
NM_001172128.1:c.312+15643C=	NP_001165599.1:n.312+15643C=
NM_001172128.2:c.312+15643C=	NP_001165599.1:n.312+15643C=
NM_001352684.1:c.-1708+15643C=	NP_001339613.1:n.-1708+15643C=
NM_001352684.2:c.-1708+15643C=	NP_001339613.1:n.-1708+15643C=
NM_001352685.1:c.-347+15643C=	NP_001339614.1:n.-347+15643C=
NM_001352685.2:c.-347+15643C=	NP_001339614.1:n.-347+15643C=
NM_001352686.1:c.465+15643C=	NP_001339615.1:n.465+15643C=
NM_001352686.2:c.465+15643C=	NP_001339615.1:n.465+15643C=
NM_172217.3:c.312+15643C=	NP_757366.2:n.312+15643C=
NM_172217.4:c.312+15643C=	NP_757366.2:n.312+15643C=
NR_148035.1:n.688+15643C=
NR_148035.2:n.687+15643C=
ENST00000302987.10:c.453+15643C=	ENSP00000302935.5:n.453+15643C=
ENST00000302987.8:c.312+15643C=	ENSP00000302935.4:n.312+15643C=
ENST00000302987.9:c.453+15643C=	ENSP00000302935.5:n.453+15643C=
ENST00000360547.9:c.312+15643C=	ENSP00000456972.1:n.312+15643C=
ENST00000394660.6:c.312+15643C=	ENSP00000378155.2:n.312+15643C=
ENST00000559383.5:c.312+15643C=	ENSP00000453250.1:n.312+15643C=
ENST00000560241.5:c.312+15643C=	ENSP00000452738.1:n.312+15643C=
ENST00000706926.1:c.312+15643C=	ENSP00000516648.1:n.312+15643C=
XM_005254342.2:c.453+15643C=	XP_005254399.1:n.453+15643C=
XM_011521518.1:c.312+15643C=	XP_011519820.1:n.312+15643C=
XM_011521519.1:c.312+15643C=	XP_011519821.1:n.312+15643C=
XM_011521520.1:c.312+15643C=	XP_011519822.1:n.312+15643C=
XR_931805.1:n.413+15643C=