Canonical Allele Identifier: CA359430671

Gene: IL7R

Linked Data

• gnomAD v4: 5-35873541-T-G
• MyVariant Identifiers: chr5:g.35873643T>G (hg19) ; chr5:g.35873541T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.35873541T>G , CM000667.2:g.35873541T>G	GRCh38
NC_000005.9:g.35873643T>G , CM000667.1:g.35873643T>G	GRCh37
NC_000005.8:g.35909400T>G	NCBI36
NG_009567.1:g.21653T>G , LRG_74:g.21653T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303115.8:c.599T>G MANE Select	ENSP00000306157.3:p.Met200Arg
ENST00000303115.7:c.599T>G	ENSP00000306157.3:p.Met200Arg
ENST00000505093.1:c.8T>G	ENSP00000426069.1:p.Met3Arg
ENST00000506850.5:c.599T>G	ENSP00000421207.1:p.Met200Arg
ENST00000509668.1:n.341T>G
ENST00000514217.5:c.538-1971T>G	ENSP00000427688.1:n.538-1971T>G
NM_002185.3:c.599T>G	NP_002176.2:p.Met200Arg
NR_120485.1:n.641-1971T>G
XM_005248299.2:c.599T>G	XP_005248356.1:p.Met200Arg
XM_005248300.1:c.599T>G	XP_005248357.1:p.Met200Arg
XM_011514037.1:c.599T>G	XP_011512339.1:p.Met200Arg
NM_002185.4:c.599T>G	NP_002176.2:p.Met200Arg
NR_120485.2:n.667-1971T>G
XM_005248299.4:c.599T>G	XP_005248356.1:p.Met200Arg
NM_002185.5:c.599T>G MANE Select	NP_002176.2:p.Met200Arg
NR_120485.3:n.625-1971T>G