Canonical Allele Identifier: CA2483127594

Gene: IL10 IL19

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206773341T= , CM000663.2:g.206773341T=	GRCh38
NC_000001.10:g.206946686T= , CM000663.1:g.206946686T=	GRCh37
NC_000001.9:g.205013309T=	NCBI36
NG_012088.1:g.4154A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000659065.2:c.-15+339A= (IL10)	ENSP00000499588.1:n.-15+339A=
ENST00000659642.2:c.-1023A= (IL10)	ENSP00000499509.1:n.-1023A=
ENST00000664374.2:c.-15+989A= (IL10)	ENSP00000499664.1:n.-15+989A=
ENST00000659997.3:c.-149+2263T= (IL19) MANE Select	ENSP00000499459.2:n.-149+2263T=
ENST00000656872.2:c.-149+2511T= (IL19)	ENSP00000499487.2:n.-149+2511T=
ENST00000659065.1:c.-15+339A= (IL10)	ENSP00000499588.1:n.-15+339A=
ENST00000659642.1:c.-1023A= (IL10)	ENSP00000499509.1:n.-1023A=
ENST00000659997.2:c.-149+2263T= (IL19)	ENSP00000499459.2:n.-149+2263T=
ENST00000662320.1:n.67+2511T= (IL19)
ENST00000664374.1:c.-15+989A= (IL10)	ENSP00000499664.1:n.-15+989A=
XM_011509506.1:c.-906A= (IL10)	XP_011507808.1:n.-906A=
NM_153758.3:c.-35+2263T= (IL19)	NP_715639.1:n.-35+2263T=
NM_001393490.1:c.-149+2511T= (IL19)	NP_001380419.1:n.-149+2511T=
NM_153758.5:c.-149+2263T= (IL19) MANE Select	NP_715639.2:n.-149+2263T=