Canonical Allele Identifier: CA1888029348
Community Standard Title: NM_000417.3(IL2RA):c.301C= (p.Gln101=)
Gene: IL2RA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.6024310G= , CM000672.2:g.6024310G= GRCh38
NC_000010.10:g.6066273G= , CM000672.1:g.6066273G= GRCh37
NC_000010.9:g.6106279G= NCBI36
NG_007403.1:g.43000C= , LRG_73:g.43000C=

Transcript Alleles

HGVS Amino-acid Change
NM_000417.3:c.301C= MANE Select NP_000408.1:p.Gln101=
ENST00000379959.8:c.301C= MANE Select ENSP00000369293.3:p.Gln101=
NM_000417.2:c.301C= , LRG_73t1:c.301C= NP_000408.1:p.Gln101=
NM_001308242.1:c.301C= NP_001295171.1:p.Gln101=
NM_001308242.2:c.301C= NP_001295171.1:p.Gln101=
NM_001308243.1:c.301C= NP_001295172.1:p.Gln101=
NM_001308243.2:c.301C= NP_001295172.1:p.Gln101=
ENST00000256876.10:c.301C= ENSP00000256876.6:p.Gln101=
ENST00000379954.5:c.301C= ENSP00000369287.1:p.Gln101=
ENST00000379959.7:c.301C= ENSP00000369293.3:p.Gln101=
ENST00000447847.1:c.213C=
ENST00000447847.2:c.301C= ENSP00000402024.2:p.Gln101=
ENST00000697424.1:c.301C= ENSP00000513307.1:p.Gln101=