Canonical Allele Identifier: CA2580598062
Community Standard Title: NM_000417.3(IL2RA):c.65-13242G>C
Gene: IL2RA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.6039267C>G , CM000672.2:g.6039267C>G GRCh38
NC_000010.10:g.6081230C>G , CM000672.1:g.6081230C>G GRCh37
NC_000010.9:g.6121236C>G NCBI36
NG_007403.1:g.28043G>C , LRG_73:g.28043G>C

Transcript Alleles

HGVS Amino-acid Change
NM_000417.3:c.65-13242G>C MANE Select NP_000408.1:n.65-13242G>C
ENST00000379959.8:c.65-13242G>C MANE Select ENSP00000369293.3:n.65-13242G>C
NM_000417.2:c.65-13242G>C , LRG_73t1:c.65-13242G>C NP_000408.1:n.65-13242G>C
NM_001308242.1:c.65-13242G>C NP_001295171.1:n.65-13242G>C
NM_001308242.2:c.65-13242G>C NP_001295171.1:n.65-13242G>C
NM_001308243.1:c.65-13242G>C NP_001295172.1:n.65-13242G>C
NM_001308243.2:c.65-13242G>C NP_001295172.1:n.65-13242G>C
ENST00000256876.10:c.65-13242G>C ENSP00000256876.6:n.65-13242G>C
ENST00000379954.5:c.65-13242G>C ENSP00000369287.1:n.65-13242G>C
ENST00000379959.7:c.65-13242G>C ENSP00000369293.3:n.65-13242G>C
ENST00000447847.2:c.65-13242G>C ENSP00000402024.2:n.65-13242G>C
ENST00000697424.1:c.65-13242G>C ENSP00000513307.1:n.65-13242G>C