Canonical Allele Identifier: CA1725931394

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92494501A= , CM000669.2:g.92494501A= GRCh38
NC_000007.13:g.92123815A= , CM000669.1:g.92123815A= GRCh37
NC_000007.12:g.91961751A= NCBI36
NG_008341.1:g.39031T=
NG_008341.2:g.39031T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.2912T= (PEX1) MANE Select ENSP00000248633.4:p.Val971=
ENST00000248633.8:c.2912T= (PEX1) ENSP00000248633.4:p.Val971=
ENST00000428214.5:c.2741T= (PEX1) ENSP00000394413.1:p.Val914=
ENST00000438045.5:c.1946T= (PEX1) ENSP00000410438.1:p.Val649=
ENST00000484913.5:n.2951T= (PEX1)
ENST00000496420.5:n.2804T= (PEX1)
NM_000466.2:c.2912T= (PEX1) NP_000457.1:p.Val971=
NM_001282677.1:c.2741T= (PEX1) NP_001269606.1:p.Val914=
NM_001282678.1:c.2288T= (PEX1) NP_001269607.1:p.Val763=
XM_005250433.3:c.1163T= (PEX1) XP_005250490.1:p.Val388=
XR_242246.3:n.3008T= (PEX1)
XM_017012319.2:c.1163T= (PEX1) XP_016867808.1:p.Val388=
XR_001744808.2:n.1939T= (PEX1)
XR_001744843.2:n.5470A= (GATAD1)
XR_242246.5:n.2959T= (PEX1)
XR_927494.3:n.4321A= (GATAD1)
XR_927503.3:n.4252A= (GATAD1)
NM_000466.3:c.2912T= (PEX1) MANE Select NP_000457.1:p.Val971=
NM_001282677.2:c.2741T= (PEX1) NP_001269606.1:p.Val914=
NM_001282678.2:c.2288T= (PEX1) NP_001269607.1:p.Val763=