Canonical Allele Identifier: CA456624297
Gene: PEX1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.92146869T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92517555T>C , CM000669.2:g.92517555T>C GRCh38
NC_000007.13:g.92146869T>C , CM000669.1:g.92146869T>C GRCh37
NC_000007.12:g.91984805T>C NCBI36
NG_008341.1:g.15977A>G
NG_008341.2:g.15977A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.960A>G MANE Select ENSP00000248633.4:p.Glu320=
ENST00000248633.8:c.960A>G ENSP00000248633.4:p.Glu320=
ENST00000428214.5:c.960A>G ENSP00000394413.1:p.Glu320=
ENST00000438045.5:c.274-3588A>G ENSP00000410438.1:n.274-3588A>G
ENST00000484913.5:n.999A>G
NM_000466.2:c.960A>G NP_000457.1:p.Glu320=
NM_001282677.1:c.960A>G NP_001269606.1:p.Glu320=
NM_001282678.1:c.336A>G NP_001269607.1:p.Glu112=
XR_242246.3:n.1056A>G
XM_017012319.2:c.-707A>G XP_016867808.1:n.-707A>G
XR_001744808.2:n.70A>G
XR_242246.5:n.1007A>G
NM_000466.3:c.960A>G MANE Select NP_000457.1:p.Glu320=
NM_001282677.2:c.960A>G NP_001269606.1:p.Glu320=
NM_001282678.2:c.336A>G NP_001269607.1:p.Glu112=