Canonical Allele Identifier: CA2673534952

Gene: IL7R

Linked Data

• dbSNP Id: rs2149899328
• gnomAD v4: 5-35867496-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.35867500del , CM000667.2:g.35867500del	GRCh38
NC_000005.9:g.35867602del , CM000667.1:g.35867602del	GRCh37
NC_000005.8:g.35903359del	NCBI36
NG_009567.1:g.15612del , LRG_74:g.15612del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303115.8:c.379+37del MANE Select	ENSP00000306157.3:n.379+37del
ENST00000303115.7:c.379+37del	ENSP00000306157.3:n.379+37del
ENST00000506850.5:c.379+37del	ENSP00000421207.1:n.379+37del
ENST00000511982.1:c.416del	ENSP00000425309.1:p.Leu139TrpfsTer4
ENST00000514217.5:c.379+37del	ENSP00000427688.1:n.379+37del
NM_002185.3:c.379+37del	NP_002176.2:n.379+37del
NR_120485.1:n.482+37del
XM_005248299.2:c.379+37del	XP_005248356.1:n.379+37del
XM_005248300.1:c.379+37del	XP_005248357.1:n.379+37del
XM_011514037.1:c.379+37del	XP_011512339.1:n.379+37del
NM_002185.4:c.379+37del	NP_002176.2:n.379+37del
NR_120485.2:n.508+37del
XM_005248299.4:c.379+37del	XP_005248356.1:n.379+37del
NM_002185.5:c.379+37del MANE Select	NP_002176.2:n.379+37del
NR_120485.3:n.466+37del