Canonical Allele Identifier: CA359430976

Gene: IL7R

Linked Data

• MyVariant Identifiers: chr5:g.35873702T>C (hg19) ; chr5:g.35873600T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.35873600T>C , CM000667.2:g.35873600T>C	GRCh38
NC_000005.9:g.35873702T>C , CM000667.1:g.35873702T>C	GRCh37
NC_000005.8:g.35909459T>C	NCBI36
NG_009567.1:g.21712T>C , LRG_74:g.21712T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000303115.8:c.658T>C MANE Select	ENSP00000306157.3:p.Trp220Arg
ENST00000303115.7:c.658T>C	ENSP00000306157.3:p.Trp220Arg
ENST00000505093.1:c.67T>C	ENSP00000426069.1:p.Trp23Arg
ENST00000506850.5:c.658T>C	ENSP00000421207.1:p.Trp220Arg
ENST00000509668.1:n.400T>C
ENST00000514217.5:c.538-1912T>C	ENSP00000427688.1:n.538-1912T>C
NM_002185.3:c.658T>C	NP_002176.2:p.Trp220Arg
NR_120485.1:n.641-1912T>C
XM_005248299.2:c.658T>C	XP_005248356.1:p.Trp220Arg
XM_005248300.1:c.658T>C	XP_005248357.1:p.Trp220Arg
XM_011514037.1:c.658T>C	XP_011512339.1:p.Trp220Arg
NM_002185.4:c.658T>C	NP_002176.2:p.Trp220Arg
NR_120485.2:n.667-1912T>C
XM_005248299.4:c.658T>C	XP_005248356.1:p.Trp220Arg
NM_002185.5:c.658T>C MANE Select	NP_002176.2:p.Trp220Arg
NR_120485.3:n.625-1912T>C