Canonical Allele Identifier: CA160129
Community Standard Title: NM_002185.5(IL7R):c.1092T>G (p.Asp364Glu)
Gene: IL7R HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.35876198T>G , CM000667.2:g.35876198T>G GRCh38
NC_000005.9:g.35876300T>G , CM000667.1:g.35876300T>G GRCh37
NC_000005.8:g.35912057T>G NCBI36
NG_009567.1:g.24310T>G , LRG_74:g.24310T>G

Transcript Alleles

HGVS Amino-acid Change
NM_002185.5:c.1092T>G MANE Select NP_002176.2:p.Asp364Glu
ENST00000303115.8:c.1092T>G MANE Select ENSP00000306157.3:p.Asp364Glu
NM_002185.3:c.1092T>G NP_002176.2:p.Asp364Glu
NM_002185.4:c.1092T>G NP_002176.2:p.Asp364Glu
NR_120485.1:n.932T>G
NR_120485.2:n.958T>G
NR_120485.3:n.916T>G
ENST00000303115.7:c.1092T>G ENSP00000306157.3:p.Asp364Glu
ENST00000505093.1:c.407T>G ENSP00000426069.1:n.407T>G
ENST00000505875.1:n.390T>G
ENST00000514217.5:c.*286T>G ENSP00000427688.1:n.*286T>G
XM_005248299.4:c.*209T>G XP_005248356.1:n.*209T>G
Search 100 bp 5'
Search 100 bp 3'