Canonical Allele Identifier: CA1718075378
Gene: CCL26 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.75769591C= , CM000669.2:g.75769591C= GRCh38
NC_000007.13:g.75398909C= , CM000669.1:g.75398909C= GRCh37
NC_000007.12:g.75236845C= NCBI36
NG_015989.1:g.25156G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000005180.9:c.*102G= MANE Select ENSP00000005180.4:n.*102G=
ENST00000005180.8:c.*102G= ENSP00000005180.4:n.*102G=
ENST00000394905.2:c.*102G= ENSP00000378365.2:n.*102G=
NM_006072.4:c.*102G= NP_006063.1:n.*102G=
XM_017011671.1:c.*102G= XP_016867160.1:n.*102G=
XM_017011672.1:c.*102G= XP_016867161.1:n.*102G=
NM_001371936.1:c.*102G= NP_001358865.1:n.*102G=
NM_001371938.1:c.*102G= MANE Select NP_001358867.1:n.*102G=