Canonical Allele Identifier: CA2739265485
Gene: PEX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2830447
ClinVar RCV Id: RCV003758253

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92496713del , CM000669.2:g.92496713del GRCh38
NC_000007.13:g.92126027del , CM000669.1:g.92126027del GRCh37
NC_000007.12:g.91963963del NCBI36
NG_008341.1:g.36820del
NG_008341.2:g.36820del

Transcript Alleles

HGVS Amino-acid change
ENST00000248633.9:c.2783+1del
ENST00000248633.8:c.2783+1del
ENST00000428214.5:c.2612+1del
ENST00000438045.5:c.1817+1del
ENST00000484913.5:n.2822+1del
ENST00000496420.5:n.2675+1del
NM_000466.2:c.2783+1del
NM_001282677.1:c.2612+1del
NM_001282678.1:c.2159+1del
XM_005250433.3:c.1034+1del
XR_242246.3:n.2879+1del
XM_017012319.2:c.1034+1del
XR_001744808.2:n.1810+1del
XR_242246.5:n.2830+1del
NM_000466.3:c.2783+1del
NM_001282677.2:c.2612+1del
NM_001282678.2:c.2159+1del