Canonical Allele Identifier: CA456624214

Linked Data

MyVariant Identifiers: chr7:g.92120763A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92491449A>C , CM000669.2:g.92491449A>C GRCh38
NC_000007.13:g.92120763A>C , CM000669.1:g.92120763A>C GRCh37
NC_000007.12:g.91958699A>C NCBI36
NG_008341.1:g.42083T>G
NG_008341.2:g.42083T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.3261T>G (PEX1) MANE Select ENSP00000248633.4:p.Leu1087=
ENST00000248633.8:c.3261T>G (PEX1) ENSP00000248633.4:p.Leu1087=
ENST00000428214.5:c.3090T>G (PEX1) ENSP00000394413.1:p.Leu1030=
ENST00000438045.5:c.2295T>G (PEX1) ENSP00000410438.1:p.Leu765=
ENST00000484913.5:n.3300T>G (PEX1)
ENST00000496420.5:n.4316T>G (PEX1)
NM_000466.2:c.3261T>G (PEX1) NP_000457.1:p.Leu1087=
NM_001282677.1:c.3090T>G (PEX1) NP_001269606.1:p.Leu1030=
NM_001282678.1:c.2637T>G (PEX1) NP_001269607.1:p.Leu879=
XM_005250433.3:c.1512T>G (PEX1) XP_005250490.1:p.Leu504=
XR_242246.3:n.3357T>G (PEX1)
XM_017012319.2:c.1512T>G (PEX1) XP_016867808.1:p.Leu504=
XR_001744808.2:n.2288T>G (PEX1)
XR_001744842.2:n.2487A>C (GATAD1)
XR_001744843.2:n.2418A>C (GATAD1)
XR_002956472.1:n.2544A>C (GATAD1)
XR_002956473.1:n.2575A>C (GATAD1)
XR_002956474.1:n.2492A>C (GATAD1)
XR_242246.5:n.3308T>G (PEX1)
XR_927494.3:n.1269A>C (GATAD1)
XR_927500.3:n.1266A>C (GATAD1)
XR_927503.3:n.1200A>C (GATAD1)
NM_000466.3:c.3261T>G (PEX1) MANE Select NP_000457.1:p.Leu1087=
NM_001282677.2:c.3090T>G (PEX1) NP_001269606.1:p.Leu1030=
NM_001282678.2:c.2637T>G (PEX1) NP_001269607.1:p.Leu879=