Canonical Allele Identifier: CA359431436

Gene: IL7R

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.35874447A>G , CM000667.2:g.35874447A>G	GRCh38
NC_000005.9:g.35874549A>G , CM000667.1:g.35874549A>G	GRCh37
NC_000005.8:g.35910306A>G	NCBI36
NG_009567.1:g.22559A>G , LRG_74:g.22559A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_002185.5:c.707-2A>G MANE Select	NP_002176.2:n.707-2A>G
ENST00000303115.8:c.707-2A>G MANE Select	ENSP00000306157.3:n.707-2A>G
NM_002185.3:c.707-2A>G	NP_002176.2:n.707-2A>G
NM_002185.4:c.707-2A>G	NP_002176.2:n.707-2A>G
NR_120485.1:n.641-1065A>G
NR_120485.2:n.667-1065A>G
NR_120485.3:n.625-1065A>G
ENST00000303115.7:c.707-2A>G	ENSP00000306157.3:n.707-2A>G
ENST00000505093.1:c.115+799A>G	ENSP00000426069.1:n.115+799A>G
ENST00000506850.5:c.706+799A>G	ENSP00000421207.1:n.706+799A>G
ENST00000509668.1:n.449-2A>G
ENST00000514217.5:c.538-1065A>G	ENSP00000427688.1:n.538-1065A>G
XM_005248299.2:c.706+799A>G	XP_005248356.1:n.706+799A>G
XM_005248299.4:c.706+799A>G	XP_005248356.1:n.706+799A>G
XM_005248300.1:c.706+799A>G	XP_005248357.1:n.706+799A>G
XM_011514037.1:c.707-2A>G	XP_011512339.1:n.707-2A>G