Canonical Allele Identifier: CA456624400
Gene: PEX1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.92147298A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92517984A>G , CM000669.2:g.92517984A>G GRCh38
NC_000007.13:g.92147298A>G , CM000669.1:g.92147298A>G GRCh37
NC_000007.12:g.91985234A>G NCBI36
NG_008341.1:g.15548T>C
NG_008341.2:g.15548T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.531T>C MANE Select ENSP00000248633.4:p.Ile177=
ENST00000248633.8:c.531T>C ENSP00000248633.4:p.Ile177=
ENST00000428214.5:c.531T>C ENSP00000394413.1:p.Ile177=
ENST00000438045.5:c.274-4017T>C ENSP00000410438.1:n.274-4017T>C
ENST00000484913.5:n.570T>C
NM_000466.2:c.531T>C NP_000457.1:p.Ile177=
NM_001282677.1:c.531T>C NP_001269606.1:p.Ile177=
NM_001282678.1:c.-94T>C NP_001269607.1:n.-94T>C
XR_242246.3:n.627T>C
XR_242246.5:n.578T>C
NM_000466.3:c.531T>C MANE Select NP_000457.1:p.Ile177=
NM_001282677.2:c.531T>C NP_001269606.1:p.Ile177=
NM_001282678.2:c.-94T>C NP_001269607.1:n.-94T>C