Canonical Allele Identifier: CA3231903

Gene: IL7R

Linked Data

• dbSNP Id: rs751425932
• ExAC: 5:35867484 TTAC / T
• MyVariant Identifiers: chr5:g.35867485_35867487del (hg19) ; chr5:g.35867383_35867385del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.35867384_35867386del , CM000667.2:g.35867384_35867386del	GRCh38
NC_000005.9:g.35867486_35867488del , CM000667.1:g.35867486_35867488del	GRCh37
NC_000005.8:g.35903243_35903245del	NCBI36
NG_009567.1:g.15496_15498del , LRG_74:g.15496_15498del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303115.8:c.300_302del MANE Select	ENSP00000306157.3:p.Leu101del
ENST00000303115.7:c.300_302del	ENSP00000306157.3:p.Leu101del
ENST00000506850.5:c.300_302del	ENSP00000421207.1:p.Leu101del
ENST00000511031.1:n.434_436del
ENST00000511982.1:c.300_302del	ENSP00000425309.1:p.Leu101del
ENST00000514217.5:c.300_302del	ENSP00000427688.1:p.Leu101del
NM_002185.3:c.300_302del	NP_002176.2:p.Leu101del
NR_120485.1:n.403_405del
XM_005248299.2:c.300_302del	XP_005248356.1:p.Leu101del
XM_005248300.1:c.300_302del	XP_005248357.1:p.Leu101del
XM_011514037.1:c.300_302del	XP_011512339.1:p.Leu101del
NM_002185.4:c.300_302del	NP_002176.2:p.Leu101del
NR_120485.2:n.429_431del
XM_005248299.4:c.300_302del	XP_005248356.1:p.Leu101del
NM_002185.5:c.300_302del MANE Select	NP_002176.2:p.Leu101del
NR_120485.3:n.387_389del