Canonical Allele Identifier: CA344482150

Gene: IL10 IL19

Linked Data

• MyVariant Identifiers: chr1:g.206944359G>T (hg19) ; chr1:g.206771014G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206771014G>T , CM000663.2:g.206771014G>T	GRCh38
NC_000001.10:g.206944359G>T , CM000663.1:g.206944359G>T	GRCh37
NC_000001.9:g.205010982G>T	NCBI36
NG_012088.1:g.6481C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367099.4:n.176C>A (IL10)
ENST00000471071.2:c.16C>A (IL10)	ENSP00000493073.2:p.Leu6Met
ENST00000659065.2:c.154C>A (IL10)	ENSP00000499588.1:p.Leu52Met
ENST00000659642.2:c.154C>A (IL10)	ENSP00000499509.1:p.Leu52Met
ENST00000664374.2:c.154C>A (IL10)	ENSP00000499664.1:p.Leu52Met
ENST00000659997.3:c.-213G>T (IL19) MANE Select	ENSP00000499459.2:n.-213G>T
ENST00000656872.2:c.-149+184G>T (IL19)	ENSP00000499487.2:n.-149+184G>T
ENST00000659065.1:c.154C>A (IL10)	ENSP00000499588.1:p.Leu52Met
ENST00000659642.1:c.154C>A (IL10)	ENSP00000499509.1:p.Leu52Met
ENST00000659997.2:c.-213G>T (IL19)	ENSP00000499459.2:n.-213G>T
ENST00000662320.1:n.67+184G>T (IL19)
ENST00000664374.1:c.154C>A (IL10)	ENSP00000499664.1:p.Leu52Met
ENST00000367099.3:n.176C>A (IL10)
ENST00000423557.1:c.271C>A (IL10) MANE Select	ENSP00000412237.1:p.Leu91Met
ENST00000471071.1:n.186C>A (IL10)
NM_000572.2:c.271C>A (IL10)	NP_000563.1:p.Leu91Met
XM_011509506.1:c.271C>A (IL10)	XP_011507808.1:p.Leu91Met
NM_000572.3:c.271C>A (IL10) MANE Select	NP_000563.1:p.Leu91Met
NM_153758.3:c.-99G>T (IL19)	NP_715639.1:n.-99G>T
NM_001382624.1:c.16C>A (IL10)	NP_001369553.1:p.Leu6Met
NM_001393490.1:c.-149+184G>T (IL19)	NP_001380419.1:n.-149+184G>T
NM_153758.5:c.-213G>T (IL19) MANE Select	NP_715639.2:n.-213G>T
NR_168466.1:n.330C>A (IL10)