Canonical Allele Identifier: CA2683369142

Gene: CCL26

Linked Data

• gnomAD v4: 7-75769693-TCA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.75769696_75769697del , CM000669.2:g.75769696_75769697del	GRCh38
NC_000007.13:g.75399014_75399015del , CM000669.1:g.75399014_75399015del	GRCh37
NC_000007.12:g.75236950_75236951del	NCBI36
NG_015989.1:g.25052_25053del

Transcript Alleles

HGVS	Amino-acid change
ENST00000005180.9:c.283_284del MANE Select	ENSP00000005180.4:p.Ter95ThrextTer28
ENST00000005180.8:c.283_284del	ENSP00000005180.4:p.Ter95ThrextTer28
ENST00000394905.2:c.283_284del	ENSP00000378365.2:p.Ter95ThrextTer28
NM_006072.4:c.283_284del	NP_006063.1:p.Ter95ThrextTer28
XM_017011671.1:c.445_446del	XP_016867160.1:p.Ter149ThrextTer28
XM_017011672.1:c.283_284del	XP_016867161.1:p.Ter95ThrextTer28
NM_001371936.1:c.283_284del	NP_001358865.1:p.Ter95ThrextTer28
NM_001371938.1:c.283_284del MANE Select	NP_001358867.1:p.Ter95ThrextTer28