Canonical Allele Identifier: CA2483127453

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.206773007T= , CM000663.2:g.206773007T= GRCh38
NC_000001.10:g.206946352T= , CM000663.1:g.206946352T= GRCh37
NC_000001.9:g.205012975T= NCBI36
NG_012088.1:g.4488A=

Transcript Alleles

HGVS Amino-acid change
ENST00000659065.2:c.-15+673A= (IL10) ENSP00000499588.1:n.-15+673A=
ENST00000659642.2:c.-689A= (IL10) ENSP00000499509.1:n.-689A=
ENST00000664374.2:c.-14-675A= (IL10) ENSP00000499664.1:n.-14-675A=
ENST00000659997.3:c.-149+1929T= (IL19) MANE Select ENSP00000499459.2:n.-149+1929T=
ENST00000656872.2:c.-149+2177T= (IL19) ENSP00000499487.2:n.-149+2177T=
ENST00000659065.1:c.-15+673A= (IL10) ENSP00000499588.1:n.-15+673A=
ENST00000659642.1:c.-689A= (IL10) ENSP00000499509.1:n.-689A=
ENST00000659997.2:c.-149+1929T= (IL19) ENSP00000499459.2:n.-149+1929T=
ENST00000662320.1:n.67+2177T= (IL19)
ENST00000664374.1:c.-14-675A= (IL10) ENSP00000499664.1:n.-14-675A=
XM_011509506.1:c.-572A= (IL10) XP_011507808.1:n.-572A=
NM_153758.3:c.-35+1929T= (IL19) NP_715639.1:n.-35+1929T=
NM_001393490.1:c.-149+2177T= (IL19) NP_001380419.1:n.-149+2177T=
NM_153758.5:c.-149+1929T= (IL19) MANE Select NP_715639.2:n.-149+1929T=