Canonical Allele Identifier: CA344482048

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.206770968T>G , CM000663.2:g.206770968T>G GRCh38
NC_000001.10:g.206944313T>G , CM000663.1:g.206944313T>G GRCh37
NC_000001.9:g.205010936T>G NCBI36
NG_012088.1:g.6527A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000367099.4:n.222A>C (IL10)
ENST00000471071.2:c.62A>C (IL10) ENSP00000493073.2:p.Lys21Thr
ENST00000659065.2:c.200A>C (IL10) ENSP00000499588.1:p.Lys67Thr
ENST00000659642.2:c.200A>C (IL10) ENSP00000499509.1:p.Lys67Thr
ENST00000664374.2:c.200A>C (IL10) ENSP00000499664.1:p.Lys67Thr
ENST00000659997.3:c.-259T>G (IL19) MANE Select ENSP00000499459.2:n.-259T>G
ENST00000656872.2:c.-149+138T>G (IL19) ENSP00000499487.2:n.-149+138T>G
ENST00000659065.1:c.200A>C (IL10) ENSP00000499588.1:p.Lys67Thr
ENST00000659642.1:c.200A>C (IL10) ENSP00000499509.1:p.Lys67Thr
ENST00000659997.2:c.-259T>G (IL19) ENSP00000499459.2:n.-259T>G
ENST00000662320.1:n.67+138T>G (IL19)
ENST00000664374.1:c.200A>C (IL10) ENSP00000499664.1:p.Lys67Thr
ENST00000367099.3:n.222A>C (IL10)
ENST00000423557.1:c.317A>C (IL10) MANE Select ENSP00000412237.1:p.Lys106Thr
ENST00000471071.1:n.232A>C (IL10)
NM_000572.2:c.317A>C (IL10) NP_000563.1:p.Lys106Thr
XM_011509506.1:c.317A>C (IL10) XP_011507808.1:p.Lys106Thr
NM_000572.3:c.317A>C (IL10) MANE Select NP_000563.1:p.Lys106Thr
NM_153758.3:c.-145T>G (IL19) NP_715639.1:n.-145T>G
NM_001382624.1:c.62A>C (IL10) NP_001369553.1:p.Lys21Thr
NM_001393490.1:c.-149+138T>G (IL19) NP_001380419.1:n.-149+138T>G
NM_153758.5:c.-259T>G (IL19) MANE Select NP_715639.2:n.-259T>G
NR_168466.1:n.376A>C (IL10)