Canonical Allele Identifier: CA1718075401
Gene: CCL26 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.75769622C= , CM000669.2:g.75769622C= GRCh38
NC_000007.13:g.75398940C= , CM000669.1:g.75398940C= GRCh37
NC_000007.12:g.75236876C= NCBI36
NG_015989.1:g.25125G=

Transcript Alleles

HGVS Amino-acid change
ENST00000005180.9:c.*71G= MANE Select ENSP00000005180.4:n.*71G=
ENST00000005180.8:c.*71G= ENSP00000005180.4:n.*71G=
ENST00000394905.2:c.*71G= ENSP00000378365.2:n.*71G=
NM_006072.4:c.*71G= NP_006063.1:n.*71G=
XM_017011671.1:c.*71G= XP_016867160.1:n.*71G=
XM_017011672.1:c.*71G= XP_016867161.1:n.*71G=
NM_001371936.1:c.*71G= NP_001358865.1:n.*71G=
NM_001371938.1:c.*71G= MANE Select NP_001358867.1:n.*71G=