Canonical Allele Identifier: CA1718075450
Gene: CCL26 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.75769692G= , CM000669.2:g.75769692G= GRCh38
NC_000007.13:g.75399010G= , CM000669.1:g.75399010G= GRCh37
NC_000007.12:g.75236946G= NCBI36
NG_015989.1:g.25055C=

Transcript Alleles

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