Canonical Allele Identifier: CA1414981831
Gene: IL12A HGNC NCBI
IL12A-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.159992603G= , CM000665.2:g.159992603G= GRCh38
NC_000003.11:g.159710390G= , CM000665.1:g.159710390G= GRCh37
NC_000003.10:g.161193084G= NCBI36
NG_033022.1:g.8768G=

Transcript Alleles

HGVS Amino-acid Change
NM_001397992.1:c.163-409G= (IL12A) MANE Select NP_001384921.1:n.163-409G=
ENST00000699704.1:c.163-409G= (IL12A) MANE Select ENSP00000514529.1:n.163-409G=
NM_000882.3:c.265-409G= (IL12A) NP_000873.2:n.265-409G=
NM_000882.4:c.265-409G= (IL12A) NP_000873.2:n.265-409G=
NM_001354582.1:c.265-409G= (IL12A) NP_001341511.1:n.265-409G=
NM_001354582.2:c.265-409G= (IL12A) NP_001341511.1:n.265-409G=
NM_001354583.1:c.265-848G= (IL12A) NP_001341512.1:n.265-848G=
NM_001354583.2:c.265-848G= (IL12A) NP_001341512.1:n.265-848G=
NR_108088.1:n.1153+1634C= (IL12A-AS1)
ENST00000305579.6:c.265-409G= (IL12A) ENSP00000303231.2:n.265-409G=
ENST00000305579.7:c.265-409G= (IL12A) ENSP00000303231.2:n.265-409G=
ENST00000466512.1:c.265-409G= (IL12A) ENSP00000419046.1:n.265-409G=
ENST00000468862.5:n.461-409G= (IL12A)
ENST00000480787.5:c.265-848G= (IL12A) ENSP00000420184.1:n.265-848G=
ENST00000496308.1:n.452-409G= (IL12A)