Canonical Allele Identifier: CA456480538

Linked Data

MyVariant Identifiers: chr7:g.92119078G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92489764G>A , CM000669.2:g.92489764G>A GRCh38
NC_000007.13:g.92119078G>A , CM000669.1:g.92119078G>A GRCh37
NC_000007.12:g.91957014G>A NCBI36
NG_008341.1:g.43768C>T
NG_008341.2:g.43768C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.3586C>T (PEX1) MANE Select ENSP00000248633.4:p.Leu1196=
ENST00000248633.8:c.3586C>T (PEX1) ENSP00000248633.4:p.Leu1196=
ENST00000428214.5:c.3415C>T (PEX1) ENSP00000394413.1:p.Leu1139=
ENST00000438045.5:c.2620C>T (PEX1) ENSP00000410438.1:p.Leu874=
ENST00000469417.1:n.483C>T (PEX1)
ENST00000477342.1:n.31C>T (PEX1)
ENST00000484913.5:n.3625C>T (PEX1)
ENST00000496420.5:n.4641C>T (PEX1)
NM_000466.2:c.3586C>T (PEX1) NP_000457.1:p.Leu1196=
NM_001282677.1:c.3415C>T (PEX1) NP_001269606.1:p.Leu1139=
NM_001282678.1:c.2962C>T (PEX1) NP_001269607.1:p.Leu988=
XM_005250433.3:c.1837C>T (PEX1) XP_005250490.1:p.Leu613=
XR_242246.3:n.3682C>T (PEX1)
XR_927494.1:n.1036-1479G>A (GATAD1)
XR_927495.1:n.1036-322G>A (GATAD1)
XR_927496.1:n.1041-1479G>A (GATAD1)
XR_927497.1:n.1036-322G>A (GATAD1)
XR_927498.1:n.1124-1479G>A (GATAD1)
XR_927500.1:n.1033-1479G>A (GATAD1)
XR_927502.1:n.1033-322G>A (GATAD1)
XR_927503.1:n.967-1479G>A (GATAD1)
XM_017012319.2:c.1837C>T (PEX1) XP_016867808.1:p.Leu613=
XR_001744808.2:n.2613C>T (PEX1)
XR_001744842.2:n.2281-1479G>A (GATAD1)
XR_001744843.2:n.2212-1479G>A (GATAD1)
XR_002956472.1:n.2281-322G>A (GATAD1)
XR_002956473.1:n.2369-1479G>A (GATAD1)
XR_002956474.1:n.2286-1479G>A (GATAD1)
XR_242246.5:n.3633C>T (PEX1)
XR_927494.3:n.1063-1479G>A (GATAD1)
XR_927500.3:n.1060-1479G>A (GATAD1)
XR_927503.3:n.994-1479G>A (GATAD1)
NM_000466.3:c.3586C>T (PEX1) MANE Select NP_000457.1:p.Leu1196=
NM_001282677.2:c.3415C>T (PEX1) NP_001269606.1:p.Leu1139=
NM_001282678.2:c.2962C>T (PEX1) NP_001269607.1:p.Leu988=