Canonical Allele Identifier: CA368163625

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92491333T>G , CM000669.2:g.92491333T>G GRCh38
NC_000007.13:g.92120647T>G , CM000669.1:g.92120647T>G GRCh37
NC_000007.12:g.91958583T>G NCBI36
NG_008341.1:g.42199A>C
NG_008341.2:g.42199A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.3377A>C (PEX1) MANE Select ENSP00000248633.4:p.Tyr1126Ser
ENST00000248633.8:c.3377A>C (PEX1) ENSP00000248633.4:p.Tyr1126Ser
ENST00000428214.5:c.3206A>C (PEX1) ENSP00000394413.1:p.Tyr1069Ser
ENST00000438045.5:c.2411A>C (PEX1) ENSP00000410438.1:p.Tyr804Ser
ENST00000484913.5:n.3416A>C (PEX1)
ENST00000496420.5:n.4432A>C (PEX1)
NM_000466.2:c.3377A>C (PEX1) NP_000457.1:p.Tyr1126Ser
NM_001282677.1:c.3206A>C (PEX1) NP_001269606.1:p.Tyr1069Ser
NM_001282678.1:c.2753A>C (PEX1) NP_001269607.1:p.Tyr918Ser
XM_005250433.3:c.1628A>C (PEX1) XP_005250490.1:p.Tyr543Ser
XR_242246.3:n.3473A>C (PEX1)
XM_017012319.2:c.1628A>C (PEX1) XP_016867808.1:p.Tyr543Ser
XR_001744808.2:n.2404A>C (PEX1)
XR_001744842.2:n.2371T>G (GATAD1)
XR_001744843.2:n.2302T>G (GATAD1)
XR_002956472.1:n.2428T>G (GATAD1)
XR_002956473.1:n.2459T>G (GATAD1)
XR_002956474.1:n.2376T>G (GATAD1)
XR_242246.5:n.3424A>C (PEX1)
XR_927494.3:n.1153T>G (GATAD1)
XR_927500.3:n.1150T>G (GATAD1)
XR_927503.3:n.1084T>G (GATAD1)
NM_000466.3:c.3377A>C (PEX1) MANE Select NP_000457.1:p.Tyr1126Ser
NM_001282677.2:c.3206A>C (PEX1) NP_001269606.1:p.Tyr1069Ser
NM_001282678.2:c.2753A>C (PEX1) NP_001269607.1:p.Tyr918Ser