Canonical Allele Identifier: CA36556716

Gene: IL24

Linked Data - Predicted Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206901560T>A , CM000663.2:g.206901560T>A	GRCh38
NC_000001.10:g.207074905T>A , CM000663.1:g.207074905T>A	GRCh37
NC_000001.9:g.205141528T>A	NCBI36
NG_029565.1:g.9118T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000294984.7:c.370T>A MANE Select	ENSP00000294984.2:p.Tyr124Asn
ENST00000294984.6:c.370T>A	ENSP00000294984.2:p.Tyr124Asn
ENST00000367093.3:c.307-438T>A	ENSP00000356060.3:n.307-438T>A
ENST00000367095.7:c.*18T>A	ENSP00000356062.3:n.*18T>A
ENST00000391929.7:c.373T>A	ENSP00000375795.3:p.Tyr125Asn
ENST00000480741.1:c.108-438T>A	ENSP00000418933.1:n.108-438T>A
ENST00000491169.1:n.281T>A
ENST00000611909.4:c.108-438T>A	ENSP00000484900.1:n.108-438T>A
NM_001185156.1:c.373T>A	NP_001172085.1:p.Tyr125Asn
NM_001185157.1:c.307-438T>A	NP_001172086.1:n.307-438T>A
NM_001185158.1:c.108-438T>A	NP_001172087.1:n.108-438T>A
NM_006850.3:c.370T>A MANE Select	NP_006841.1:p.Tyr124Asn
XM_011509101.1:c.289T>A	XP_011507403.1:p.Tyr97Asn
XM_011509101.2:c.289T>A	XP_011507403.1:p.Tyr97Asn
XM_017000121.1:c.289T>A	XP_016855610.1:p.Tyr97Asn