Canonical Allele Identifier: CA124396

Gene: IL7R

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.35873593G>A , CM000667.2:g.35873593G>A	GRCh38
NC_000005.9:g.35873695G>A , CM000667.1:g.35873695G>A	GRCh37
NC_000005.8:g.35909452G>A	NCBI36
NG_009567.1:g.21705G>A , LRG_74:g.21705G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303115.8:c.651G>A MANE Select	ENSP00000306157.3:p.Trp217Ter
ENST00000303115.7:c.651G>A	ENSP00000306157.3:p.Trp217Ter
ENST00000505093.1:c.60G>A	ENSP00000426069.1:p.Trp20Ter
ENST00000506850.5:c.651G>A	ENSP00000421207.1:p.Trp217Ter
ENST00000509668.1:n.393G>A
ENST00000514217.5:c.538-1919G>A	ENSP00000427688.1:n.538-1919G>A
NM_002185.3:c.651G>A	NP_002176.2:p.Trp217Ter
NR_120485.1:n.641-1919G>A
XM_005248299.2:c.651G>A	XP_005248356.1:p.Trp217Ter
XM_005248300.1:c.651G>A	XP_005248357.1:p.Trp217Ter
XM_011514037.1:c.651G>A	XP_011512339.1:p.Trp217Ter
NM_002185.4:c.651G>A	NP_002176.2:p.Trp217Ter
NR_120485.2:n.667-1919G>A
XM_005248299.4:c.651G>A	XP_005248356.1:p.Trp217Ter
NM_002185.5:c.651G>A MANE Select	NP_002176.2:p.Trp217Ter
NR_120485.3:n.625-1919G>A