Canonical Allele Identifier: CA368168464

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92494527G>C , CM000669.2:g.92494527G>C GRCh38
NC_000007.13:g.92123841G>C , CM000669.1:g.92123841G>C GRCh37
NC_000007.12:g.91961777G>C NCBI36
NG_008341.1:g.39005C>G
NG_008341.2:g.39005C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000248633.9:c.2886C>G (PEX1) MANE Select ENSP00000248633.4:p.Asn962Lys
ENST00000248633.8:c.2886C>G (PEX1) ENSP00000248633.4:p.Asn962Lys
ENST00000428214.5:c.2715C>G (PEX1) ENSP00000394413.1:p.Asn905Lys
ENST00000438045.5:c.1920C>G (PEX1) ENSP00000410438.1:p.Asn640Lys
ENST00000484913.5:n.2925C>G (PEX1)
ENST00000496420.5:n.2778C>G (PEX1)
NM_000466.2:c.2886C>G (PEX1) NP_000457.1:p.Asn962Lys
NM_001282677.1:c.2715C>G (PEX1) NP_001269606.1:p.Asn905Lys
NM_001282678.1:c.2262C>G (PEX1) NP_001269607.1:p.Asn754Lys
XM_005250433.3:c.1137C>G (PEX1) XP_005250490.1:p.Asn379Lys
XR_242246.3:n.2982C>G (PEX1)
XM_017012319.2:c.1137C>G (PEX1) XP_016867808.1:p.Asn379Lys
XR_001744808.2:n.1913C>G (PEX1)
XR_001744843.2:n.5496G>C (GATAD1)
XR_242246.5:n.2933C>G (PEX1)
XR_927494.3:n.4347G>C (GATAD1)
XR_927503.3:n.4278G>C (GATAD1)
NM_000466.3:c.2886C>G (PEX1) MANE Select NP_000457.1:p.Asn962Lys
NM_001282677.2:c.2715C>G (PEX1) NP_001269606.1:p.Asn905Lys
NM_001282678.2:c.2262C>G (PEX1) NP_001269607.1:p.Asn754Lys