Canonical Allele Identifier: CA15848550

Gene: IL16

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.81293722C>T , CM000677.2:g.81293722C>T	GRCh38
NC_000015.9:g.81586063C>T , CM000677.1:g.81586063C>T	GRCh37
NC_000015.8:g.79373118C>T	NCBI36
NG_029933.1:g.101845C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302987.10:c.2043+685C>T	ENSP00000302935.5:n.2043+685C>T
ENST00000706926.1:c.1902+685C>T	ENSP00000516648.1:n.1902+685C>T
ENST00000302987.9:c.2043+685C>T	ENSP00000302935.5:n.2043+685C>T
ENST00000683961.1:c.1902+685C>T MANE Select	ENSP00000508085.1:n.1902+685C>T
ENST00000302987.8:c.1902+685C>T	ENSP00000302935.4:n.1902+685C>T
ENST00000360547.9:c.*1079+685C>T	ENSP00000456972.1:n.*1079+685C>T
ENST00000394660.6:c.1902+685C>T	ENSP00000378155.2:n.1902+685C>T
ENST00000560115.5:c.1683+685C>T
NM_001172128.1:c.1902+685C>T	NP_001165599.1:n.1902+685C>T
NM_172217.3:c.1902+685C>T	NP_757366.2:n.1902+685C>T
XM_005254342.2:c.2043+685C>T	XP_005254399.1:n.2043+685C>T
XM_011521518.1:c.1764+823C>T	XP_011519820.1:n.1764+823C>T
XM_011521519.1:c.1902+685C>T	XP_011519821.1:n.1902+685C>T
XM_011521520.1:c.1902+685C>T	XP_011519822.1:n.1902+685C>T
XR_931805.1:n.2003+685C>T
NM_001352684.1:c.-118+685C>T	NP_001339613.1:n.-118+685C>T
NM_001352685.1:c.1392+685C>T	NP_001339614.1:n.1392+685C>T
NM_001352686.1:c.2055+685C>T	NP_001339615.1:n.2055+685C>T
NM_172217.4:c.1902+685C>T	NP_757366.2:n.1902+685C>T
NR_148035.1:n.2278+685C>T
NM_001172128.2:c.1902+685C>T	NP_001165599.1:n.1902+685C>T
NM_001352684.2:c.-118+685C>T	NP_001339613.1:n.-118+685C>T
NM_001352685.2:c.1392+685C>T	NP_001339614.1:n.1392+685C>T
NM_172217.5:c.1902+685C>T MANE Select	NP_757366.2:n.1902+685C>T
NR_148035.2:n.2277+685C>T
NM_001352686.2:c.2055+685C>T	NP_001339615.1:n.2055+685C>T