Canonical Allele Identifier: CA359431053

Gene: IL7R

Linked Data

• MyVariant Identifiers: chr5:g.35873716T>A (hg19) ; chr5:g.35873614T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.35873614T>A , CM000667.2:g.35873614T>A	GRCh38
NC_000005.9:g.35873716T>A , CM000667.1:g.35873716T>A	GRCh37
NC_000005.8:g.35909473T>A	NCBI36
NG_009567.1:g.21726T>A , LRG_74:g.21726T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303115.8:c.672T>A MANE Select	ENSP00000306157.3:p.Tyr224Ter
ENST00000303115.7:c.672T>A	ENSP00000306157.3:p.Tyr224Ter
ENST00000505093.1:c.81T>A	ENSP00000426069.1:p.Tyr27Ter
ENST00000506850.5:c.672T>A	ENSP00000421207.1:p.Tyr224Ter
ENST00000509668.1:n.414T>A
ENST00000514217.5:c.538-1898T>A	ENSP00000427688.1:n.538-1898T>A
NM_002185.3:c.672T>A	NP_002176.2:p.Tyr224Ter
NR_120485.1:n.641-1898T>A
XM_005248299.2:c.672T>A	XP_005248356.1:p.Tyr224Ter
XM_005248300.1:c.672T>A	XP_005248357.1:p.Tyr224Ter
XM_011514037.1:c.672T>A	XP_011512339.1:p.Tyr224Ter
NM_002185.4:c.672T>A	NP_002176.2:p.Tyr224Ter
NR_120485.2:n.667-1898T>A
XM_005248299.4:c.672T>A	XP_005248356.1:p.Tyr224Ter
NM_002185.5:c.672T>A MANE Select	NP_002176.2:p.Tyr224Ter
NR_120485.3:n.625-1898T>A