Canonical Allele Identifier: CA1139895353

Gene: IL10 IL19

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206773552T= , CM000663.2:g.206773552T=	GRCh38
NC_000001.10:g.206946897T= , CM000663.1:g.206946897T=	GRCh37
NC_000001.9:g.205013520T=	NCBI36
NG_012088.1:g.3943A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000659065.2:c.-15+128A= (IL10)	ENSP00000499588.1:n.-15+128A=
ENST00000659642.2:c.-1118-116A= (IL10)	ENSP00000499509.1:n.-1118-116A=
ENST00000664374.2:c.-15+778A= (IL10)	ENSP00000499664.1:n.-15+778A=
ENST00000659997.3:c.-149+2474T= (IL19) MANE Select	ENSP00000499459.2:n.-149+2474T=
ENST00000656872.2:c.-149+2722T= (IL19)	ENSP00000499487.2:n.-149+2722T=
ENST00000659065.1:c.-15+128A= (IL10)	ENSP00000499588.1:n.-15+128A=
ENST00000659642.1:c.-1118-116A= (IL10)	ENSP00000499509.1:n.-1118-116A=
ENST00000659997.2:c.-149+2474T= (IL19)	ENSP00000499459.2:n.-149+2474T=
ENST00000662320.1:n.67+2722T= (IL19)
ENST00000664374.1:c.-15+778A= (IL10)	ENSP00000499664.1:n.-15+778A=
XM_011509506.1:c.-1001-116A= (IL10)	XP_011507808.1:n.-1001-116A=
NM_153758.3:c.-35+2474T= (IL19)	NP_715639.1:n.-35+2474T=
NM_001393490.1:c.-149+2722T= (IL19)	NP_001380419.1:n.-149+2722T=
NM_153758.5:c.-149+2474T= (IL19) MANE Select	NP_715639.2:n.-149+2474T=