Canonical Allele Identifier: CA1718075395

Gene: CCL26

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.75769610T= , CM000669.2:g.75769610T=	GRCh38
NC_000007.13:g.75398928T= , CM000669.1:g.75398928T=	GRCh37
NC_000007.12:g.75236864T=	NCBI36
NG_015989.1:g.25137A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000005180.9:c.*83A= MANE Select	ENSP00000005180.4:n.*83A=
ENST00000005180.8:c.*83A=	ENSP00000005180.4:n.*83A=
ENST00000394905.2:c.*83A=	ENSP00000378365.2:n.*83A=
NM_006072.4:c.*83A=	NP_006063.1:n.*83A=
XM_017011671.1:c.*83A=	XP_016867160.1:n.*83A=
XM_017011672.1:c.*83A=	XP_016867161.1:n.*83A=
NM_001371936.1:c.*83A=	NP_001358865.1:n.*83A=
NM_001371938.1:c.*83A= MANE Select	NP_001358867.1:n.*83A=