Canonical Allele Identifier: CA2519757146
Gene: CCL26 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.75769582_75769585dup , CM000669.2:g.75769582_75769585dup GRCh38
NC_000007.13:g.75398900_75398903dup , CM000669.1:g.75398900_75398903dup GRCh37
NC_000007.12:g.75236836_75236839dup NCBI36
NG_015989.1:g.25163_25166dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000005180.9:c.*109_*112dup MANE Select ENSP00000005180.4:n.*109_*112dup
ENST00000005180.8:c.*109_*112dup ENSP00000005180.4:n.*109_*112dup
ENST00000394905.2:c.*109_*112dup ENSP00000378365.2:n.*109_*112dup
NM_006072.4:c.*109_*112dup NP_006063.1:n.*109_*112dup
XM_017011671.1:c.*109_*112dup XP_016867160.1:n.*109_*112dup
XM_017011672.1:c.*109_*112dup XP_016867161.1:n.*109_*112dup
NM_001371936.1:c.*109_*112dup NP_001358865.1:n.*109_*112dup
NM_001371938.1:c.*109_*112dup MANE Select NP_001358867.1:n.*109_*112dup