Canonical Allele Identifier: CA1583211276
Gene: IL5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132544224A= , CM000667.2:g.132544224A= GRCh38
NC_000005.9:g.131879916A= , CM000667.1:g.131879916A= GRCh37
NC_000005.8:g.131907815A= NCBI36
NG_033019.1:g.4299T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000450655.1:c.43-1098T= ENSP00000409825.1:n.43-1098T=
ENST00000638452.2:c.-168-15060A= ENSP00000492349.2:n.-168-15060A=
ENST00000638504.1:n.207-15060A=
ENST00000638568.2:c.-310-12108A= ENSP00000491158.2:n.-310-12108A=
ENST00000639899.1:n.290-15060A=
ENST00000640655.2:c.-168-15060A= ENSP00000491596.2:n.-168-15060A=
XM_005271988.2:c.43-722T= XP_005272045.1:n.43-722T=
XM_005271988.4:c.43-722T= XP_005272045.1:n.43-722T=
XM_006714601.2:c.43-665T= XP_006714664.1:n.43-665T=
XM_011543373.1:c.-24-722T= XP_011541675.1:n.-24-722T=
XM_011543373.3:c.-24-722T= XP_011541675.1:n.-24-722T=
XM_011543374.1:c.-77-669T= XP_011541676.1:n.-77-669T=
XM_011543374.3:c.-77-669T= XP_011541676.1:n.-77-669T=
XM_011543375.1:c.43-1098T= XP_011541677.1:n.43-1098T=