Canonical Allele Identifier: CA368167611

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92494360A>G , CM000669.2:g.92494360A>G GRCh38
NC_000007.13:g.92123674A>G , CM000669.1:g.92123674A>G GRCh37
NC_000007.12:g.91961610A>G NCBI36
NG_008341.1:g.39172T>C
NG_008341.2:g.39172T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.2963T>C (PEX1) MANE Select ENSP00000248633.4:p.Leu988Ser
ENST00000248633.8:c.2963T>C (PEX1) ENSP00000248633.4:p.Leu988Ser
ENST00000428214.5:c.2792T>C (PEX1) ENSP00000394413.1:p.Leu931Ser
ENST00000438045.5:c.1997T>C (PEX1) ENSP00000410438.1:p.Leu666Ser
ENST00000484913.5:n.3002T>C (PEX1)
ENST00000496420.5:n.2855T>C (PEX1)
NM_000466.2:c.2963T>C (PEX1) NP_000457.1:p.Leu988Ser
NM_001282677.1:c.2792T>C (PEX1) NP_001269606.1:p.Leu931Ser
NM_001282678.1:c.2339T>C (PEX1) NP_001269607.1:p.Leu780Ser
XM_005250433.3:c.1214T>C (PEX1) XP_005250490.1:p.Leu405Ser
XR_242246.3:n.3059T>C (PEX1)
XM_017012319.2:c.1214T>C (PEX1) XP_016867808.1:p.Leu405Ser
XR_001744808.2:n.1990T>C (PEX1)
XR_001744843.2:n.5329A>G (GATAD1)
XR_242246.5:n.3010T>C (PEX1)
XR_927494.3:n.4180A>G (GATAD1)
XR_927503.3:n.4111A>G (GATAD1)
NM_000466.3:c.2963T>C (PEX1) MANE Select NP_000457.1:p.Leu988Ser
NM_001282677.2:c.2792T>C (PEX1) NP_001269606.1:p.Leu931Ser
NM_001282678.2:c.2339T>C (PEX1) NP_001269607.1:p.Leu780Ser