Canonical Allele Identifier: CA2673534983
Gene: IL7R HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.35867600_35867609del , CM000667.2:g.35867600_35867609del GRCh38
NC_000005.9:g.35867702_35867711del , CM000667.1:g.35867702_35867711del GRCh37
NC_000005.8:g.35903459_35903468del NCBI36
NG_009567.1:g.15712_15721del , LRG_74:g.15712_15721del

Transcript Alleles

HGVS Amino-acid Change
ENST00000303115.8:c.379+137_379+146del MANE Select ENSP00000306157.3:n.379+137_379+146del
ENST00000303115.7:c.379+137_379+146del ENSP00000306157.3:n.379+137_379+146del
ENST00000506850.5:c.379+137_379+146del ENSP00000421207.1:n.379+137_379+146del
ENST00000511982.1:c.*63_*72del ENSP00000425309.1:n.*63_*72del
ENST00000514217.5:c.379+137_379+146del ENSP00000427688.1:n.379+137_379+146del
NM_002185.3:c.379+137_379+146del NP_002176.2:n.379+137_379+146del
NR_120485.1:n.482+137_482+146del
XM_005248299.2:c.379+137_379+146del XP_005248356.1:n.379+137_379+146del
XM_005248300.1:c.379+137_379+146del XP_005248357.1:n.379+137_379+146del
XM_011514037.1:c.379+137_379+146del XP_011512339.1:n.379+137_379+146del
NM_002185.4:c.379+137_379+146del NP_002176.2:n.379+137_379+146del
NR_120485.2:n.508+137_508+146del
XM_005248299.4:c.379+137_379+146del XP_005248356.1:n.379+137_379+146del
NM_002185.5:c.379+137_379+146del MANE Select NP_002176.2:n.379+137_379+146del
NR_120485.3:n.466+137_466+146del