Canonical Allele Identifier: CA359430931
Gene: IL7R HGNC NCBI

Linked Data

COSMIC: COSM4402565
MyVariant Identifiers: chr5:g.35873694G>A (hg19) chr5:g.35873592G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.35873592G>A , CM000667.2:g.35873592G>A GRCh38
NC_000005.9:g.35873694G>A , CM000667.1:g.35873694G>A GRCh37
NC_000005.8:g.35909451G>A NCBI36
NG_009567.1:g.21704G>A , LRG_74:g.21704G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000303115.8:c.650G>A MANE Select ENSP00000306157.3:p.Trp217Ter
ENST00000303115.7:c.650G>A ENSP00000306157.3:p.Trp217Ter
ENST00000505093.1:c.59G>A ENSP00000426069.1:p.Trp20Ter
ENST00000506850.5:c.650G>A ENSP00000421207.1:p.Trp217Ter
ENST00000509668.1:n.392G>A
ENST00000514217.5:c.538-1920G>A ENSP00000427688.1:n.538-1920G>A
NM_002185.3:c.650G>A NP_002176.2:p.Trp217Ter
NR_120485.1:n.641-1920G>A
XM_005248299.2:c.650G>A XP_005248356.1:p.Trp217Ter
XM_005248300.1:c.650G>A XP_005248357.1:p.Trp217Ter
XM_011514037.1:c.650G>A XP_011512339.1:p.Trp217Ter
NM_002185.4:c.650G>A NP_002176.2:p.Trp217Ter
NR_120485.2:n.667-1920G>A
XM_005248299.4:c.650G>A XP_005248356.1:p.Trp217Ter
NM_002185.5:c.650G>A MANE Select NP_002176.2:p.Trp217Ter
NR_120485.3:n.625-1920G>A
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