Canonical Allele Identifier: CA2573157697
Gene: PEX26 HGNC NCBI

Linked Data

dbSNP Id: rs2123643634

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.18078374_18078377del , CM000684.2:g.18078374_18078377del GRCh38
NC_000022.10:g.18561140_18561143del , CM000684.1:g.18561140_18561143del GRCh37
NC_000022.9:g.16941140_16941143del NCBI36
NG_008339.1:g.5455_5458del

Transcript Alleles

HGVS Amino-acid Change
ENST00000399744.8:c.-3_1del
ENST00000474897.6:c.-3_1del
ENST00000329627.11:c.-3_1del
ENST00000399744.7:c.-3_1del
ENST00000474897.5:c.-3_1del
ENST00000610387.4:c.-3_1del
NM_001127649.2:c.-3_1del
NM_001199319.1:c.-3_1del
NM_017929.5:c.-3_1del
NM_001127649.3:c.-3_1del
NM_001199319.2:c.-3_1del
NM_017929.6:c.-3_1del