Canonical Allele Identifier: CA2673534950

Gene: IL7R

Linked Data

• gnomAD v4: 5-35867409-GT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.35867410del , CM000667.2:g.35867410del	GRCh38
NC_000005.9:g.35867512del , CM000667.1:g.35867512del	GRCh37
NC_000005.8:g.35903269del	NCBI36
NG_009567.1:g.15522del , LRG_74:g.15522del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303115.8:c.326del MANE Select	ENSP00000306157.3:p.Val109GlyfsTer8
ENST00000303115.7:c.326del	ENSP00000306157.3:p.Val109GlyfsTer8
ENST00000506850.5:c.326del	ENSP00000421207.1:p.Val109GlyfsTer8
ENST00000511031.1:n.460del
ENST00000511982.1:c.326del	ENSP00000425309.1:p.Val109GlyfsTer8
ENST00000514217.5:c.326del	ENSP00000427688.1:p.Val109GlyfsTer8
NM_002185.3:c.326del	NP_002176.2:p.Val109GlyfsTer8
NR_120485.1:n.429del
XM_005248299.2:c.326del	XP_005248356.1:p.Val109GlyfsTer8
XM_005248300.1:c.326del	XP_005248357.1:p.Val109GlyfsTer8
XM_011514037.1:c.326del	XP_011512339.1:p.Val109GlyfsTer8
NM_002185.4:c.326del	NP_002176.2:p.Val109GlyfsTer8
NR_120485.2:n.455del
XM_005248299.4:c.326del	XP_005248356.1:p.Val109GlyfsTer8
NM_002185.5:c.326del MANE Select	NP_002176.2:p.Val109GlyfsTer8
NR_120485.3:n.413del