Canonical Allele Identifier: CA1539052309
Gene: IL7R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.35873515G= , CM000667.2:g.35873515G= GRCh38
NC_000005.9:g.35873617G= , CM000667.1:g.35873617G= GRCh37
NC_000005.8:g.35909374G= NCBI36
NG_009567.1:g.21627G= , LRG_74:g.21627G=

Transcript Alleles

HGVS Amino-acid change
ENST00000303115.8:c.573G= MANE Select ENSP00000306157.3:p.Leu191=
ENST00000303115.7:c.573G= ENSP00000306157.3:p.Leu191=
ENST00000506850.5:c.573G= ENSP00000421207.1:p.Leu191=
ENST00000509668.1:n.315G=
ENST00000514217.5:c.538-1997G= ENSP00000427688.1:n.538-1997G=
NM_002185.3:c.573G= NP_002176.2:p.Leu191=
NR_120485.1:n.641-1997G=
XM_005248299.2:c.573G= XP_005248356.1:p.Leu191=
XM_005248300.1:c.573G= XP_005248357.1:p.Leu191=
XM_011514037.1:c.573G= XP_011512339.1:p.Leu191=
NM_002185.4:c.573G= NP_002176.2:p.Leu191=
NR_120485.2:n.667-1997G=
XM_005248299.4:c.573G= XP_005248356.1:p.Leu191=
NM_002185.5:c.573G= MANE Select NP_002176.2:p.Leu191=
NR_120485.3:n.625-1997G=