Canonical Allele Identifier: CA368163909

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92491367C>G , CM000669.2:g.92491367C>G GRCh38
NC_000007.13:g.92120681C>G , CM000669.1:g.92120681C>G GRCh37
NC_000007.12:g.91958617C>G NCBI36
NG_008341.1:g.42165G>C
NG_008341.2:g.42165G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.3343G>C (PEX1) MANE Select ENSP00000248633.4:p.Glu1115Gln
ENST00000248633.8:c.3343G>C (PEX1) ENSP00000248633.4:p.Glu1115Gln
ENST00000428214.5:c.3172G>C (PEX1) ENSP00000394413.1:p.Glu1058Gln
ENST00000438045.5:c.2377G>C (PEX1) ENSP00000410438.1:p.Glu793Gln
ENST00000484913.5:n.3382G>C (PEX1)
ENST00000496420.5:n.4398G>C (PEX1)
NM_000466.2:c.3343G>C (PEX1) NP_000457.1:p.Glu1115Gln
NM_001282677.1:c.3172G>C (PEX1) NP_001269606.1:p.Glu1058Gln
NM_001282678.1:c.2719G>C (PEX1) NP_001269607.1:p.Glu907Gln
XM_005250433.3:c.1594G>C (PEX1) XP_005250490.1:p.Glu532Gln
XR_242246.3:n.3439G>C (PEX1)
XM_017012319.2:c.1594G>C (PEX1) XP_016867808.1:p.Glu532Gln
XR_001744808.2:n.2370G>C (PEX1)
XR_001744842.2:n.2405C>G (GATAD1)
XR_001744843.2:n.2336C>G (GATAD1)
XR_002956472.1:n.2462C>G (GATAD1)
XR_002956473.1:n.2493C>G (GATAD1)
XR_002956474.1:n.2410C>G (GATAD1)
XR_242246.5:n.3390G>C (PEX1)
XR_927494.3:n.1187C>G (GATAD1)
XR_927500.3:n.1184C>G (GATAD1)
XR_927503.3:n.1118C>G (GATAD1)
NM_000466.3:c.3343G>C (PEX1) MANE Select NP_000457.1:p.Glu1115Gln
NM_001282677.2:c.3172G>C (PEX1) NP_001269606.1:p.Glu1058Gln
NM_001282678.2:c.2719G>C (PEX1) NP_001269607.1:p.Glu907Gln