Canonical Allele Identifier: CA2499219046

Linked Data

ClinVar Variation Id: 1154126
ClinVar RCV Id: RCV001496012
dbSNP Id: rs2116092636

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92494406A>T , CM000669.2:g.92494406A>T GRCh38
NC_000007.13:g.92123720A>T , CM000669.1:g.92123720A>T GRCh37
NC_000007.12:g.91961656A>T NCBI36
NG_008341.1:g.39126T>A
NG_008341.2:g.39126T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000248633.9:c.2927-10T>A (PEX1) MANE Select ENSP00000248633.4:n.2927-10T>A
ENST00000248633.8:c.2927-10T>A (PEX1) ENSP00000248633.4:n.2927-10T>A
ENST00000428214.5:c.2756-10T>A (PEX1) ENSP00000394413.1:n.2756-10T>A
ENST00000438045.5:c.1961-10T>A (PEX1) ENSP00000410438.1:n.1961-10T>A
ENST00000484913.5:n.2966-10T>A (PEX1)
ENST00000496420.5:n.2819-10T>A (PEX1)
NM_000466.2:c.2927-10T>A (PEX1) NP_000457.1:n.2927-10T>A
NM_001282677.1:c.2756-10T>A (PEX1) NP_001269606.1:n.2756-10T>A
NM_001282678.1:c.2303-10T>A (PEX1) NP_001269607.1:n.2303-10T>A
XM_005250433.3:c.1178-10T>A (PEX1) XP_005250490.1:n.1178-10T>A
XR_242246.3:n.3023-10T>A (PEX1)
XM_017012319.2:c.1178-10T>A (PEX1) XP_016867808.1:n.1178-10T>A
XR_001744808.2:n.1954-10T>A (PEX1)
XR_001744843.2:n.5375A>T (GATAD1)
XR_242246.5:n.2974-10T>A (PEX1)
XR_927494.3:n.4226A>T (GATAD1)
XR_927503.3:n.4157A>T (GATAD1)
NM_000466.3:c.2927-10T>A (PEX1) MANE Select NP_000457.1:n.2927-10T>A
NM_001282677.2:c.2756-10T>A (PEX1) NP_001269606.1:n.2756-10T>A
NM_001282678.2:c.2303-10T>A (PEX1) NP_001269607.1:n.2303-10T>A