Canonical Allele Identifier: CA2776946747
Gene: PEX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92506409_92506410insACA , CM000669.2:g.92506409_92506410insACA GRCh38
NC_000007.13:g.92135723_92135724insACA , CM000669.1:g.92135723_92135724insACA GRCh37
NC_000007.12:g.91973659_91973660insACA NCBI36
NG_008341.1:g.27122_27123insTGT
NG_008341.2:g.27122_27123insTGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.1804-66_1804-65insTGT MANE Select ENSP00000248633.4:n.1804-66_1804-65insTGT
ENST00000248633.8:c.1804-66_1804-65insTGT ENSP00000248633.4:n.1804-66_1804-65insTGT
ENST00000422866.1:c.622-66_622-65insTGT
ENST00000428214.5:c.1804-66_1804-65insTGT ENSP00000394413.1:n.1804-66_1804-65insTGT
ENST00000438045.5:c.838-66_838-65insTGT ENSP00000410438.1:n.838-66_838-65insTGT
ENST00000484913.5:n.1843-66_1843-65insTGT
ENST00000496420.5:n.1414_1415insTGT
NM_000466.2:c.1804-66_1804-65insTGT NP_000457.1:n.1804-66_1804-65insTGT
NM_001282677.1:c.1804-66_1804-65insTGT NP_001269606.1:n.1804-66_1804-65insTGT
NM_001282678.1:c.1180-66_1180-65insTGT NP_001269607.1:n.1180-66_1180-65insTGT
XM_005250433.3:c.55-66_55-65insTGT XP_005250490.1:n.55-66_55-65insTGT
XR_242246.3:n.1900-66_1900-65insTGT
XM_017012319.2:c.55-66_55-65insTGT XP_016867808.1:n.55-66_55-65insTGT
XR_001744808.2:n.831-66_831-65insTGT
XR_242246.5:n.1851-66_1851-65insTGT
NM_000466.3:c.1804-66_1804-65insTGT MANE Select NP_000457.1:n.1804-66_1804-65insTGT
NM_001282677.2:c.1804-66_1804-65insTGT NP_001269606.1:n.1804-66_1804-65insTGT
NM_001282678.2:c.1180-66_1180-65insTGT NP_001269607.1:n.1180-66_1180-65insTGT