Canonical Allele Identifier: CA456481534

Linked Data

MyVariant Identifiers: chr7:g.92123802C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92494488C>T , CM000669.2:g.92494488C>T GRCh38
NC_000007.13:g.92123802C>T , CM000669.1:g.92123802C>T GRCh37
NC_000007.12:g.91961738C>T NCBI36
NG_008341.1:g.39044G>A
NG_008341.2:g.39044G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.2925G>A (PEX1) MANE Select ENSP00000248633.4:p.Gln975=
ENST00000248633.8:c.2925G>A (PEX1) ENSP00000248633.4:p.Gln975=
ENST00000428214.5:c.2754G>A (PEX1) ENSP00000394413.1:p.Gln918=
ENST00000438045.5:c.1959G>A (PEX1) ENSP00000410438.1:p.Gln653=
ENST00000484913.5:n.2964G>A (PEX1)
ENST00000496420.5:n.2817G>A (PEX1)
NM_000466.2:c.2925G>A (PEX1) NP_000457.1:p.Gln975=
NM_001282677.1:c.2754G>A (PEX1) NP_001269606.1:p.Gln918=
NM_001282678.1:c.2301G>A (PEX1) NP_001269607.1:p.Gln767=
XM_005250433.3:c.1176G>A (PEX1) XP_005250490.1:p.Gln392=
XR_242246.3:n.3021G>A (PEX1)
XM_017012319.2:c.1176G>A (PEX1) XP_016867808.1:p.Gln392=
XR_001744808.2:n.1952G>A (PEX1)
XR_001744843.2:n.5457C>T (GATAD1)
XR_242246.5:n.2972G>A (PEX1)
XR_927494.3:n.4308C>T (GATAD1)
XR_927503.3:n.4239C>T (GATAD1)
NM_000466.3:c.2925G>A (PEX1) MANE Select NP_000457.1:p.Gln975=
NM_001282677.2:c.2754G>A (PEX1) NP_001269606.1:p.Gln918=
NM_001282678.2:c.2301G>A (PEX1) NP_001269607.1:p.Gln767=