Canonical Allele Identifier: CA646375359

Gene: IL10 IL19

Linked Data

• COSMIC: COSN7199535

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206771884C>T , CM000663.2:g.206771884C>T	GRCh38
NC_000001.10:g.206945229C>T , CM000663.1:g.206945229C>T	GRCh37
NC_000001.9:g.205011852C>T	NCBI36
NG_012088.1:g.5611G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000659065.2:c.48+387G>A (IL10)	ENSP00000499588.1:n.48+387G>A
ENST00000659642.2:c.48+387G>A (IL10)	ENSP00000499509.1:n.48+387G>A
ENST00000664374.2:c.48+387G>A (IL10)	ENSP00000499664.1:n.48+387G>A
ENST00000659997.3:c.-149+806C>T (IL19) MANE Select	ENSP00000499459.2:n.-149+806C>T
ENST00000656872.2:c.-149+1054C>T (IL19)	ENSP00000499487.2:n.-149+1054C>T
ENST00000659065.1:c.48+387G>A (IL10)	ENSP00000499588.1:n.48+387G>A
ENST00000659642.1:c.48+387G>A (IL10)	ENSP00000499509.1:n.48+387G>A
ENST00000659997.2:c.-149+806C>T (IL19)	ENSP00000499459.2:n.-149+806C>T
ENST00000662320.1:n.67+1054C>T (IL19)
ENST00000664374.1:c.48+387G>A (IL10)	ENSP00000499664.1:n.48+387G>A
ENST00000423557.1:c.165+387G>A (IL10) MANE Select	ENSP00000412237.1:n.165+387G>A
NM_000572.2:c.165+387G>A (IL10)	NP_000563.1:n.165+387G>A
XM_011509506.1:c.165+387G>A (IL10)	XP_011507808.1:n.165+387G>A
NM_000572.3:c.165+387G>A (IL10) MANE Select	NP_000563.1:n.165+387G>A
NM_153758.3:c.-35+806C>T (IL19)	NP_715639.1:n.-35+806C>T
NM_001393490.1:c.-149+1054C>T (IL19)	NP_001380419.1:n.-149+1054C>T
NM_153758.5:c.-149+806C>T (IL19) MANE Select	NP_715639.2:n.-149+806C>T
NR_168466.1:n.224+387G>A (IL10)