Canonical Allele Identifier: CA1539080315
Gene: IL7R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.35875988A= , CM000667.2:g.35875988A= GRCh38
NC_000005.9:g.35876090A= , CM000667.1:g.35876090A= GRCh37
NC_000005.8:g.35911847A= NCBI36
NG_009567.1:g.24100A= , LRG_74:g.24100A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000303115.8:c.882A= MANE Select ENSP00000306157.3:p.Leu294=
ENST00000303115.7:c.882A= ENSP00000306157.3:p.Leu294=
ENST00000505093.1:c.197A= ENSP00000426069.1:p.Ter66=
ENST00000505875.1:n.180A=
ENST00000514217.5:c.*76A= ENSP00000427688.1:n.*76A=
NM_002185.3:c.882A= NP_002176.2:p.Leu294=
NR_120485.1:n.722A=
XM_005248299.2:c.788A= XP_005248356.1:p.Ter263=
NM_002185.4:c.882A= NP_002176.2:p.Leu294=
NR_120485.2:n.748A=
XM_005248299.4:c.788A= XP_005248356.1:p.Ter263=
NM_002185.5:c.882A= MANE Select NP_002176.2:p.Leu294=
NR_120485.3:n.706A=