Canonical Allele Identifier: CA359428653

Gene: IL7R

Linked Data

• COSMIC: COSM394810
• MyVariant Identifiers: chr5:g.35867560C>A (hg19) ; chr5:g.35867458C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.35867458C>A , CM000667.2:g.35867458C>A	GRCh38
NC_000005.9:g.35867560C>A , CM000667.1:g.35867560C>A	GRCh37
NC_000005.8:g.35903317C>A	NCBI36
NG_009567.1:g.15570C>A , LRG_74:g.15570C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303115.8:c.374C>A MANE Select	ENSP00000306157.3:p.Thr125Asn
ENST00000303115.7:c.374C>A	ENSP00000306157.3:p.Thr125Asn
ENST00000506850.5:c.374C>A	ENSP00000421207.1:p.Thr125Asn
ENST00000511031.1:n.508C>A
ENST00000511982.1:c.374C>A	ENSP00000425309.1:p.Thr125Asn
ENST00000514217.5:c.374C>A	ENSP00000427688.1:p.Thr125Asn
NM_002185.3:c.374C>A	NP_002176.2:p.Thr125Asn
NR_120485.1:n.477C>A
XM_005248299.2:c.374C>A	XP_005248356.1:p.Thr125Asn
XM_005248300.1:c.374C>A	XP_005248357.1:p.Thr125Asn
XM_011514037.1:c.374C>A	XP_011512339.1:p.Thr125Asn
NM_002185.4:c.374C>A	NP_002176.2:p.Thr125Asn
NR_120485.2:n.503C>A
XM_005248299.4:c.374C>A	XP_005248356.1:p.Thr125Asn
NM_002185.5:c.374C>A MANE Select	NP_002176.2:p.Thr125Asn
NR_120485.3:n.461C>A