Canonical Allele Identifier: CA1718075379
Gene: CCL26 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.75769592A= , CM000669.2:g.75769592A= GRCh38
NC_000007.13:g.75398910A= , CM000669.1:g.75398910A= GRCh37
NC_000007.12:g.75236846A= NCBI36
NG_015989.1:g.25155T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000005180.9:c.*101T= MANE Select ENSP00000005180.4:n.*101T=
ENST00000005180.8:c.*101T= ENSP00000005180.4:n.*101T=
ENST00000394905.2:c.*101T= ENSP00000378365.2:n.*101T=
NM_006072.4:c.*101T= NP_006063.1:n.*101T=
XM_017011671.1:c.*101T= XP_016867160.1:n.*101T=
XM_017011672.1:c.*101T= XP_016867161.1:n.*101T=
NM_001371936.1:c.*101T= NP_001358865.1:n.*101T=
NM_001371938.1:c.*101T= MANE Select NP_001358867.1:n.*101T=