Canonical Allele Identifier: CA1414986046

Gene: IL12A IL12A-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.159995680G= , CM000665.2:g.159995680G=	GRCh38
NC_000003.11:g.159713467G= , CM000665.1:g.159713467G=	GRCh37
NC_000003.10:g.161196161G=	NCBI36
NG_033022.1:g.11845G=

Transcript Alleles

HGVS	Amino-acid Change
NM_001397992.1:c.*121G= (IL12A) MANE Select	NP_001384921.1:n.*121G=
ENST00000699704.1:c.*121G= (IL12A) MANE Select	ENSP00000514529.1:n.*121G=
NM_000882.3:c.*121G= (IL12A)	NP_000873.2:n.*121G=
NM_000882.4:c.*121G= (IL12A)	NP_000873.2:n.*121G=
NM_001354582.1:c.*121G= (IL12A)	NP_001341511.1:n.*121G=
NM_001354582.2:c.*121G= (IL12A)	NP_001341511.1:n.*121G=
NM_001354583.1:c.*121G= (IL12A)	NP_001341512.1:n.*121G=
NM_001354583.2:c.*121G= (IL12A)	NP_001341512.1:n.*121G=
NR_108088.1:n.1085-1375C= (IL12A-AS1)
ENST00000305579.6:c.*121G= (IL12A)	ENSP00000303231.2:n.*121G=
ENST00000305579.7:c.*121G= (IL12A)	ENSP00000303231.2:n.*121G=
ENST00000466512.1:c.*121G= (IL12A)	ENSP00000419046.1:n.*121G=
ENST00000468862.5:n.1570G= (IL12A)