Canonical Allele Identifier: CA2505903882

Gene: IL7R

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.35857754C>A , CM000667.2:g.35857754C>A	GRCh38
NC_000005.9:g.35857856C>A , CM000667.1:g.35857856C>A	GRCh37
NC_000005.8:g.35893613C>A	NCBI36
NG_009567.1:g.5866C>A , LRG_74:g.5866C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303115.8:c.82+695C>A MANE Select	ENSP00000306157.3:n.82+695C>A
ENST00000303115.7:c.82+695C>A	ENSP00000306157.3:n.82+695C>A
ENST00000506850.5:c.82+695C>A	ENSP00000421207.1:n.82+695C>A
ENST00000508941.5:c.82+695C>A	ENSP00000426426.1:n.82+695C>A
ENST00000511031.1:n.217-3098C>A
ENST00000511982.1:c.82+695C>A	ENSP00000425309.1:n.82+695C>A
ENST00000514217.5:c.82+695C>A	ENSP00000427688.1:n.82+695C>A
ENST00000515665.1:c.82+695C>A	ENSP00000425538.1:n.82+695C>A
NM_002185.3:c.82+695C>A	NP_002176.2:n.82+695C>A
NR_120485.1:n.185+695C>A
XM_005248299.2:c.82+695C>A	XP_005248356.1:n.82+695C>A
XM_005248300.1:c.82+695C>A	XP_005248357.1:n.82+695C>A
XM_011514037.1:c.82+695C>A	XP_011512339.1:n.82+695C>A
NM_002185.4:c.82+695C>A	NP_002176.2:n.82+695C>A
NR_120485.2:n.211+695C>A
XM_005248299.4:c.82+695C>A	XP_005248356.1:n.82+695C>A
XR_001742635.1:n.1533+1113G>T
NM_002185.5:c.82+695C>A MANE Select	NP_002176.2:n.82+695C>A
NR_120485.3:n.169+695C>A