Canonical Allele Identifier: CA4340768
Community Standard Title: NM_000466.3(PEX1):c.3637-14T>C

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92489437A>G , CM000669.2:g.92489437A>G GRCh38
NC_000007.13:g.92118751A>G , CM000669.1:g.92118751A>G GRCh37
NC_000007.12:g.91956687A>G NCBI36
NG_008341.1:g.44095T>C
NG_008341.2:g.44095T>C

Transcript Alleles

HGVS Amino-acid Change
NM_000466.3:c.3637-14T>C (PEX1) MANE Select NP_000457.1:n.3637-14T>C
ENST00000248633.9:c.3637-14T>C (PEX1) MANE Select ENSP00000248633.4:n.3637-14T>C
NM_000466.2:c.3637-14T>C (PEX1) NP_000457.1:n.3637-14T>C
NM_001282677.1:c.3466-14T>C (PEX1) NP_001269606.1:n.3466-14T>C
NM_001282677.2:c.3466-14T>C (PEX1) NP_001269606.1:n.3466-14T>C
NM_001282678.1:c.3013-14T>C (PEX1) NP_001269607.1:n.3013-14T>C
NM_001282678.2:c.3013-14T>C (PEX1) NP_001269607.1:n.3013-14T>C
ENST00000248633.8:c.3637-14T>C (PEX1) ENSP00000248633.4:n.3637-14T>C
ENST00000428214.5:c.3466-14T>C (PEX1) ENSP00000394413.1:n.3466-14T>C
ENST00000438045.5:c.2671-14T>C (PEX1) ENSP00000410438.1:n.2671-14T>C
ENST00000469417.1:n.534-14T>C (PEX1)
ENST00000477342.1:n.358T>C (PEX1)
ENST00000484913.5:n.3676-14T>C (PEX1)
ENST00000496420.5:n.4687-14T>C (PEX1)
XM_005250433.3:c.1888-14T>C (PEX1) XP_005250490.1:n.1888-14T>C
XM_017012319.2:c.1888-14T>C (PEX1) XP_016867808.1:n.1888-14T>C
XR_001744808.2:n.2659-14T>C (PEX1)
XR_001744842.2:n.2281-1806A>G (GATAD1)
XR_001744843.2:n.2212-1806A>G (GATAD1)
XR_002956472.1:n.2281-649A>G (GATAD1)
XR_002956473.1:n.2369-1806A>G (GATAD1)
XR_002956474.1:n.2286-1806A>G (GATAD1)
XR_242246.3:n.3728-14T>C (PEX1)
XR_242246.5:n.3679-14T>C (PEX1)
XR_927494.1:n.1036-1806A>G (GATAD1)
XR_927494.3:n.1063-1806A>G (GATAD1)
XR_927495.1:n.1036-649A>G (GATAD1)
XR_927496.1:n.1041-1806A>G (GATAD1)
XR_927497.1:n.1036-649A>G (GATAD1)
XR_927498.1:n.1124-1806A>G (GATAD1)
XR_927500.1:n.1033-1806A>G (GATAD1)
XR_927500.3:n.1060-1806A>G (GATAD1)
XR_927502.1:n.1033-649A>G (GATAD1)
XR_927503.1:n.967-1806A>G (GATAD1)
XR_927503.3:n.994-1806A>G (GATAD1)