Canonical Allele Identifier: CA273405727

Gene: IL16

Linked Data

• dbSNP Id: rs17875491
• gnomAD v3: 15-81294587-G-A
• gnomAD v4: 15-81294587-G-A
• MyVariant Identifiers: chr15:g.81586928G>A (hg19) ; chr15:g.81294587G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.81294587G>A , CM000677.2:g.81294587G>A	GRCh38
NC_000015.9:g.81586928G>A , CM000677.1:g.81586928G>A	GRCh37
NC_000015.8:g.79373983G>A	NCBI36
NG_029933.1:g.102710G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000302987.10:c.2043+1550G>A	ENSP00000302935.5:n.2043+1550G>A
ENST00000706926.1:c.1902+1550G>A	ENSP00000516648.1:n.1902+1550G>A
ENST00000302987.9:c.2043+1550G>A	ENSP00000302935.5:n.2043+1550G>A
ENST00000683961.1:c.1902+1550G>A MANE Select	ENSP00000508085.1:n.1902+1550G>A
ENST00000302987.8:c.1902+1550G>A	ENSP00000302935.4:n.1902+1550G>A
ENST00000360547.9:c.*1079+1550G>A	ENSP00000456972.1:n.*1079+1550G>A
ENST00000394660.6:c.1902+1550G>A	ENSP00000378155.2:n.1902+1550G>A
ENST00000560115.5:c.1684-745G>A
NM_001172128.1:c.1902+1550G>A	NP_001165599.1:n.1902+1550G>A
NM_172217.3:c.1902+1550G>A	NP_757366.2:n.1902+1550G>A
XM_005254342.2:c.2043+1550G>A	XP_005254399.1:n.2043+1550G>A
XM_011521518.1:c.1764+1688G>A	XP_011519820.1:n.1764+1688G>A
XM_011521519.1:c.1902+1550G>A	XP_011519821.1:n.1902+1550G>A
XM_011521520.1:c.1902+1550G>A	XP_011519822.1:n.1902+1550G>A
XR_931805.1:n.2003+1550G>A
NM_001352684.1:c.-117-745G>A	NP_001339613.1:n.-117-745G>A
NM_001352685.1:c.1392+1550G>A	NP_001339614.1:n.1392+1550G>A
NM_001352686.1:c.2055+1550G>A	NP_001339615.1:n.2055+1550G>A
NM_172217.4:c.1902+1550G>A	NP_757366.2:n.1902+1550G>A
NR_148035.1:n.2278+1550G>A
NM_001172128.2:c.1902+1550G>A	NP_001165599.1:n.1902+1550G>A
NM_001352684.2:c.-117-745G>A	NP_001339613.1:n.-117-745G>A
NM_001352685.2:c.1392+1550G>A	NP_001339614.1:n.1392+1550G>A
NM_172217.5:c.1902+1550G>A MANE Select	NP_757366.2:n.1902+1550G>A
NR_148035.2:n.2277+1550G>A
NM_001352686.2:c.2055+1550G>A	NP_001339615.1:n.2055+1550G>A