Canonical Allele Identifier: CA1147663261

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.206771831C= , CM000663.2:g.206771831C= GRCh38
NC_000001.10:g.206945176C= , CM000663.1:g.206945176C= GRCh37
NC_000001.9:g.205011799C= NCBI36
NG_012088.1:g.5664G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000659065.2:c.49-416G= (IL10) ENSP00000499588.1:n.49-416G=
ENST00000659642.2:c.49-416G= (IL10) ENSP00000499509.1:n.49-416G=
ENST00000664374.2:c.49-416G= (IL10) ENSP00000499664.1:n.49-416G=
ENST00000659997.3:c.-149+753C= (IL19) MANE Select ENSP00000499459.2:n.-149+753C=
ENST00000656872.2:c.-149+1001C= (IL19) ENSP00000499487.2:n.-149+1001C=
ENST00000659065.1:c.49-416G= (IL10) ENSP00000499588.1:n.49-416G=
ENST00000659642.1:c.49-416G= (IL10) ENSP00000499509.1:n.49-416G=
ENST00000659997.2:c.-149+753C= (IL19) ENSP00000499459.2:n.-149+753C=
ENST00000662320.1:n.67+1001C= (IL19)
ENST00000664374.1:c.49-416G= (IL10) ENSP00000499664.1:n.49-416G=
ENST00000423557.1:c.166-416G= (IL10) MANE Select ENSP00000412237.1:n.166-416G=
NM_000572.2:c.166-416G= (IL10) NP_000563.1:n.166-416G=
XM_011509506.1:c.166-416G= (IL10) XP_011507808.1:n.166-416G=
NM_000572.3:c.166-416G= (IL10) MANE Select NP_000563.1:n.166-416G=
NM_153758.3:c.-35+753C= (IL19) NP_715639.1:n.-35+753C=
NM_001393490.1:c.-149+1001C= (IL19) NP_001380419.1:n.-149+1001C=
NM_153758.5:c.-149+753C= (IL19) MANE Select NP_715639.2:n.-149+753C=
NR_168466.1:n.225-416G= (IL10)