Canonical Allele Identifier: CA161954534
Community Standard Title: NM_000466.3(PEX1):c.3031-9T>C

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92493138A>G , CM000669.2:g.92493138A>G GRCh38
NC_000007.13:g.92122452A>G , CM000669.1:g.92122452A>G GRCh37
NC_000007.12:g.91960388A>G NCBI36
NG_008341.1:g.40394T>C
NG_008341.2:g.40394T>C

Transcript Alleles

HGVS Amino-acid Change
NM_000466.3:c.3031-9T>C (PEX1) MANE Select NP_000457.1:n.3031-9T>C
ENST00000248633.9:c.3031-9T>C (PEX1) MANE Select ENSP00000248633.4:n.3031-9T>C
NM_000466.2:c.3031-9T>C (PEX1) NP_000457.1:n.3031-9T>C
NM_001282677.1:c.2860-9T>C (PEX1) NP_001269606.1:n.2860-9T>C
NM_001282677.2:c.2860-9T>C (PEX1) NP_001269606.1:n.2860-9T>C
NM_001282678.1:c.2407-9T>C (PEX1) NP_001269607.1:n.2407-9T>C
NM_001282678.2:c.2407-9T>C (PEX1) NP_001269607.1:n.2407-9T>C
ENST00000248633.8:c.3031-9T>C (PEX1) ENSP00000248633.4:n.3031-9T>C
ENST00000428214.5:c.2860-9T>C (PEX1) ENSP00000394413.1:n.2860-9T>C
ENST00000438045.5:c.2065-9T>C (PEX1) ENSP00000410438.1:n.2065-9T>C
ENST00000484913.5:n.3070-9T>C (PEX1)
ENST00000496420.5:n.4077T>C (PEX1)
XM_005250433.3:c.1282-9T>C (PEX1) XP_005250490.1:n.1282-9T>C
XM_017012319.2:c.1282-9T>C (PEX1) XP_016867808.1:n.1282-9T>C
XR_001744808.2:n.2058-9T>C (PEX1)
XR_001744842.2:n.4176A>G (GATAD1)
XR_001744843.2:n.4107A>G (GATAD1)
XR_002956472.1:n.4233A>G (GATAD1)
XR_002956473.1:n.4264A>G (GATAD1)
XR_002956474.1:n.4181A>G (GATAD1)
XR_242246.3:n.3127-9T>C (PEX1)
XR_242246.5:n.3078-9T>C (PEX1)
XR_927494.3:n.2958A>G (GATAD1)
XR_927500.3:n.2955A>G (GATAD1)
XR_927503.3:n.2889A>G (GATAD1)