Canonical Allele Identifier: CA456481493

Linked Data

MyVariant Identifiers: chr7:g.92123688A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92494374A>T , CM000669.2:g.92494374A>T GRCh38
NC_000007.13:g.92123688A>T , CM000669.1:g.92123688A>T GRCh37
NC_000007.12:g.91961624A>T NCBI36
NG_008341.1:g.39158T>A
NG_008341.2:g.39158T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.2949T>A (PEX1) MANE Select ENSP00000248633.4:p.Thr983=
ENST00000248633.8:c.2949T>A (PEX1) ENSP00000248633.4:p.Thr983=
ENST00000428214.5:c.2778T>A (PEX1) ENSP00000394413.1:p.Thr926=
ENST00000438045.5:c.1983T>A (PEX1) ENSP00000410438.1:p.Thr661=
ENST00000484913.5:n.2988T>A (PEX1)
ENST00000496420.5:n.2841T>A (PEX1)
NM_000466.2:c.2949T>A (PEX1) NP_000457.1:p.Thr983=
NM_001282677.1:c.2778T>A (PEX1) NP_001269606.1:p.Thr926=
NM_001282678.1:c.2325T>A (PEX1) NP_001269607.1:p.Thr775=
XM_005250433.3:c.1200T>A (PEX1) XP_005250490.1:p.Thr400=
XR_242246.3:n.3045T>A (PEX1)
XM_017012319.2:c.1200T>A (PEX1) XP_016867808.1:p.Thr400=
XR_001744808.2:n.1976T>A (PEX1)
XR_001744843.2:n.5343A>T (GATAD1)
XR_242246.5:n.2996T>A (PEX1)
XR_927494.3:n.4194A>T (GATAD1)
XR_927503.3:n.4125A>T (GATAD1)
NM_000466.3:c.2949T>A (PEX1) MANE Select NP_000457.1:p.Thr983=
NM_001282677.2:c.2778T>A (PEX1) NP_001269606.1:p.Thr926=
NM_001282678.2:c.2325T>A (PEX1) NP_001269607.1:p.Thr775=