Canonical Allele Identifier: CA2673534956

Gene: IL7R

Linked Data

• gnomAD v4: 5-35867524-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.35867526del , CM000667.2:g.35867526del	GRCh38
NC_000005.9:g.35867628del , CM000667.1:g.35867628del	GRCh37
NC_000005.8:g.35903385del	NCBI36
NG_009567.1:g.15638del , LRG_74:g.15638del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303115.8:c.379+63del MANE Select	ENSP00000306157.3:n.379+63del
ENST00000303115.7:c.379+63del	ENSP00000306157.3:n.379+63del
ENST00000506850.5:c.379+63del	ENSP00000421207.1:n.379+63del
ENST00000511982.1:c.442del	ENSP00000425309.1:p.Asp148ThrfsTer10
ENST00000514217.5:c.379+63del	ENSP00000427688.1:n.379+63del
NM_002185.3:c.379+63del	NP_002176.2:n.379+63del
NR_120485.1:n.482+63del
XM_005248299.2:c.379+63del	XP_005248356.1:n.379+63del
XM_005248300.1:c.379+63del	XP_005248357.1:n.379+63del
XM_011514037.1:c.379+63del	XP_011512339.1:n.379+63del
NM_002185.4:c.379+63del	NP_002176.2:n.379+63del
NR_120485.2:n.508+63del
XM_005248299.4:c.379+63del	XP_005248356.1:n.379+63del
NM_002185.5:c.379+63del MANE Select	NP_002176.2:n.379+63del
NR_120485.3:n.466+63del