Canonical Allele Identifier: CA2483127794

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.206773732T= , CM000663.2:g.206773732T= GRCh38
NC_000001.10:g.206947077T= , CM000663.1:g.206947077T= GRCh37
NC_000001.9:g.205013700T= NCBI36
NG_012088.1:g.3763A=

Transcript Alleles

HGVS Amino-acid change
ENST00000659065.2:c.-67A= (IL10) ENSP00000499588.1:n.-67A=
ENST00000659642.2:c.-1118-296A= (IL10) ENSP00000499509.1:n.-1118-296A=
ENST00000664374.2:c.-15+598A= (IL10) ENSP00000499664.1:n.-15+598A=
ENST00000659997.3:c.-149+2654T= (IL19) MANE Select ENSP00000499459.2:n.-149+2654T=
ENST00000656872.2:c.-149+2902T= (IL19) ENSP00000499487.2:n.-149+2902T=
ENST00000659065.1:c.-67A= (IL10) ENSP00000499588.1:n.-67A=
ENST00000659642.1:c.-1118-296A= (IL10) ENSP00000499509.1:n.-1118-296A=
ENST00000659997.2:c.-149+2654T= (IL19) ENSP00000499459.2:n.-149+2654T=
ENST00000662320.1:n.67+2902T= (IL19)
ENST00000664374.1:c.-15+598A= (IL10) ENSP00000499664.1:n.-15+598A=
XM_011509506.1:c.-1001-296A= (IL10) XP_011507808.1:n.-1001-296A=
NM_153758.3:c.-35+2654T= (IL19) NP_715639.1:n.-35+2654T=
NM_001393490.1:c.-149+2902T= (IL19) NP_001380419.1:n.-149+2902T=
NM_153758.5:c.-149+2654T= (IL19) MANE Select NP_715639.2:n.-149+2654T=