Canonical Allele Identifier: CA456481547

Linked Data

MyVariant Identifiers: chr7:g.92123811T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92494497T>C , CM000669.2:g.92494497T>C GRCh38
NC_000007.13:g.92123811T>C , CM000669.1:g.92123811T>C GRCh37
NC_000007.12:g.91961747T>C NCBI36
NG_008341.1:g.39035A>G
NG_008341.2:g.39035A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.2916A>G (PEX1) MANE Select ENSP00000248633.4:p.Glu972=
ENST00000248633.8:c.2916A>G (PEX1) ENSP00000248633.4:p.Glu972=
ENST00000428214.5:c.2745A>G (PEX1) ENSP00000394413.1:p.Glu915=
ENST00000438045.5:c.1950A>G (PEX1) ENSP00000410438.1:p.Glu650=
ENST00000484913.5:n.2955A>G (PEX1)
ENST00000496420.5:n.2808A>G (PEX1)
NM_000466.2:c.2916A>G (PEX1) NP_000457.1:p.Glu972=
NM_001282677.1:c.2745A>G (PEX1) NP_001269606.1:p.Glu915=
NM_001282678.1:c.2292A>G (PEX1) NP_001269607.1:p.Glu764=
XM_005250433.3:c.1167A>G (PEX1) XP_005250490.1:p.Glu389=
XR_242246.3:n.3012A>G (PEX1)
XM_017012319.2:c.1167A>G (PEX1) XP_016867808.1:p.Glu389=
XR_001744808.2:n.1943A>G (PEX1)
XR_001744843.2:n.5466T>C (GATAD1)
XR_242246.5:n.2963A>G (PEX1)
XR_927494.3:n.4317T>C (GATAD1)
XR_927503.3:n.4248T>C (GATAD1)
NM_000466.3:c.2916A>G (PEX1) MANE Select NP_000457.1:p.Glu972=
NM_001282677.2:c.2745A>G (PEX1) NP_001269606.1:p.Glu915=
NM_001282678.2:c.2292A>G (PEX1) NP_001269607.1:p.Glu764=