Canonical Allele Identifier: CA1718075390
Gene: CCL26 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.75769602_75769605delinsTGTA , CM000669.2:g.75769602_75769605delinsTGTA GRCh38
NC_000007.13:g.75398920_75398923delinsTGTA , CM000669.1:g.75398920_75398923delinsTGTA GRCh37
NC_000007.12:g.75236856_75236859delinsTGTA NCBI36
NG_015989.1:g.25142_25145delinsTACA

Transcript Alleles

HGVS Amino-acid change
ENST00000005180.9:c.*88_*91delinsTACA MANE Select ENSP00000005180.4:n.*88_*91delinsTACA
ENST00000005180.8:c.*88_*91delinsTACA ENSP00000005180.4:n.*88_*91delinsTACA
ENST00000394905.2:c.*88_*91delinsTACA ENSP00000378365.2:n.*88_*91delinsTACA
NM_006072.4:c.*88_*91delinsTACA NP_006063.1:n.*88_*91delinsTACA
XM_017011671.1:c.*88_*91delinsTACA XP_016867160.1:n.*88_*91delinsTACA
XM_017011672.1:c.*88_*91delinsTACA XP_016867161.1:n.*88_*91delinsTACA
NM_001371936.1:c.*88_*91delinsTACA NP_001358865.1:n.*88_*91delinsTACA
NM_001371938.1:c.*88_*91delinsTACA MANE Select NP_001358867.1:n.*88_*91delinsTACA
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