Canonical Allele Identifier: CA413628244

Gene: IL2RG

Linked Data

• MyVariant Identifiers: chrX:g.70328135T>A (hg19) ; chrX:g.71108285T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71108285T>A , CM000685.2:g.71108285T>A	GRCh38
NC_000023.10:g.70328135T>A , CM000685.1:g.70328135T>A	GRCh37
NC_000023.9:g.70244860T>A	NCBI36
NG_009088.1:g.8269A>T , LRG_150:g.8269A>T
NG_021141.1:g.3504A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000482750.6:c.*36A>T	ENSP00000421262.2:n.*36A>T
ENST00000696903.1:n.1219A>T
ENST00000374202.7:c.916A>T MANE Select	ENSP00000363318.3:p.Asn306Tyr
ENST00000642473.1:n.1280A>T
ENST00000644022.1:n.1182A>T
ENST00000644708.1:n.1225A>T
ENST00000644911.1:n.1322A>T
ENST00000645266.1:c.916A>T	ENSP00000493734.1:p.Asn306Tyr
ENST00000645518.1:c.916A>T	ENSP00000493986.1:p.Asn306Tyr
ENST00000646106.1:c.916A>T	ENSP00000496437.1:p.Asn306Tyr
ENST00000646505.1:c.916A>T	ENSP00000496673.1:p.Asn306Tyr
ENST00000647492.1:c.916A>T	ENSP00000495340.1:p.Asn306Tyr
ENST00000276110.6:n.1509A>T
ENST00000374188.7:c.103A>T	ENSP00000363303.3:p.Asn35Tyr
ENST00000374202.6:c.916A>T	ENSP00000363318.2:p.Asn306Tyr
ENST00000456850.6:c.346A>T	ENSP00000388967.2:p.Asn116Tyr
ENST00000482750.5:c.232A>T
ENST00000512747.3:n.1095A>T
NM_000206.2:c.916A>T , LRG_150t1:c.916A>T	NP_000197.1:p.Asn306Tyr
NM_000206.3:c.916A>T MANE Select	NP_000197.1:p.Asn306Tyr