Canonical Allele Identifier: CA368167924

Linked Data

dbSNP Id: rs1398282085

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92494396C>G , CM000669.2:g.92494396C>G GRCh38
NC_000007.13:g.92123710C>G , CM000669.1:g.92123710C>G GRCh37
NC_000007.12:g.91961646C>G NCBI36
NG_008341.1:g.39136G>C
NG_008341.2:g.39136G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000248633.9:c.2927G>C (PEX1) MANE Select ENSP00000248633.4:p.Gly976Ala
ENST00000248633.8:c.2927G>C (PEX1) ENSP00000248633.4:p.Gly976Ala
ENST00000428214.5:c.2756G>C (PEX1) ENSP00000394413.1:p.Gly919Ala
ENST00000438045.5:c.1961G>C (PEX1) ENSP00000410438.1:p.Gly654Ala
ENST00000484913.5:n.2966G>C (PEX1)
ENST00000496420.5:n.2819G>C (PEX1)
NM_000466.2:c.2927G>C (PEX1) NP_000457.1:p.Gly976Ala
NM_001282677.1:c.2756G>C (PEX1) NP_001269606.1:p.Gly919Ala
NM_001282678.1:c.2303G>C (PEX1) NP_001269607.1:p.Gly768Ala
XM_005250433.3:c.1178G>C (PEX1) XP_005250490.1:p.Gly393Ala
XR_242246.3:n.3023G>C (PEX1)
XM_017012319.2:c.1178G>C (PEX1) XP_016867808.1:p.Gly393Ala
XR_001744808.2:n.1954G>C (PEX1)
XR_001744843.2:n.5365C>G (GATAD1)
XR_242246.5:n.2974G>C (PEX1)
XR_927494.3:n.4216C>G (GATAD1)
XR_927503.3:n.4147C>G (GATAD1)
NM_000466.3:c.2927G>C (PEX1) MANE Select NP_000457.1:p.Gly976Ala
NM_001282677.2:c.2756G>C (PEX1) NP_001269606.1:p.Gly919Ala
NM_001282678.2:c.2303G>C (PEX1) NP_001269607.1:p.Gly768Ala