Canonical Allele Identifier: CA559294565

Gene: IL7R

Linked Data

• dbSNP Id: rs869312857
• gnomAD v2: 5-35867540-CA-C
• gnomAD v4: 5-35867438-CA-C
• MyVariant Identifiers: chr5:g.35867541del (hg19) ; chr5:g.35867439del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.35867445del , CM000667.2:g.35867445del	GRCh38
NC_000005.9:g.35867547del , CM000667.1:g.35867547del	GRCh37
NC_000005.8:g.35903304del	NCBI36
NG_009567.1:g.15557del , LRG_74:g.15557del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303115.8:c.361del MANE Select	ENSP00000306157.3:p.Ile121Ter
ENST00000303115.7:c.361del	ENSP00000306157.3:p.Ile121Ter
ENST00000506850.5:c.361del	ENSP00000421207.1:p.Ile121Ter
ENST00000511031.1:n.495del
ENST00000511982.1:c.361del	ENSP00000425309.1:p.Ile121Ter
ENST00000514217.5:c.361del	ENSP00000427688.1:p.Ile121Ter
NM_002185.3:c.361del	NP_002176.2:p.Ile121Ter
NR_120485.1:n.464del
XM_005248299.2:c.361del	XP_005248356.1:p.Ile121Ter
XM_005248300.1:c.361del	XP_005248357.1:p.Ile121Ter
XM_011514037.1:c.361del	XP_011512339.1:p.Ile121Ter
NM_002185.4:c.361del	NP_002176.2:p.Ile121Ter
NR_120485.2:n.490del
XM_005248299.4:c.361del	XP_005248356.1:p.Ile121Ter
NM_002185.5:c.361del MANE Select	NP_002176.2:p.Ile121Ter
NR_120485.3:n.448del