Canonical Allele Identifier: CA2776946709
Gene: PEX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92506400_92506401insA , CM000669.2:g.92506400_92506401insA GRCh38
NC_000007.13:g.92135714_92135715insA , CM000669.1:g.92135714_92135715insA GRCh37
NC_000007.12:g.91973650_91973651insA NCBI36
NG_008341.1:g.27131_27132insT
NG_008341.2:g.27131_27132insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.1804-57_1804-56insT MANE Select ENSP00000248633.4:n.1804-57_1804-56insT
ENST00000248633.8:c.1804-57_1804-56insT ENSP00000248633.4:n.1804-57_1804-56insT
ENST00000422866.1:c.622-57_622-56insT
ENST00000428214.5:c.1804-57_1804-56insT ENSP00000394413.1:n.1804-57_1804-56insT
ENST00000438045.5:c.838-57_838-56insT ENSP00000410438.1:n.838-57_838-56insT
ENST00000484913.5:n.1843-57_1843-56insT
ENST00000496420.5:n.1423_1424insT
NM_000466.2:c.1804-57_1804-56insT NP_000457.1:n.1804-57_1804-56insT
NM_001282677.1:c.1804-57_1804-56insT NP_001269606.1:n.1804-57_1804-56insT
NM_001282678.1:c.1180-57_1180-56insT NP_001269607.1:n.1180-57_1180-56insT
XM_005250433.3:c.55-57_55-56insT XP_005250490.1:n.55-57_55-56insT
XR_242246.3:n.1900-57_1900-56insT
XM_017012319.2:c.55-57_55-56insT XP_016867808.1:n.55-57_55-56insT
XR_001744808.2:n.831-57_831-56insT
XR_242246.5:n.1851-57_1851-56insT
NM_000466.3:c.1804-57_1804-56insT MANE Select NP_000457.1:n.1804-57_1804-56insT
NM_001282677.2:c.1804-57_1804-56insT NP_001269606.1:n.1804-57_1804-56insT
NM_001282678.2:c.1180-57_1180-56insT NP_001269607.1:n.1180-57_1180-56insT