Canonical Allele Identifier: CA2776945407

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92489534_92489535insACA , CM000669.2:g.92489534_92489535insACA GRCh38
NC_000007.13:g.92118848_92118849insACA , CM000669.1:g.92118848_92118849insACA GRCh37
NC_000007.12:g.91956784_91956785insACA NCBI36
NG_008341.1:g.43997_43998insTGT
NG_008341.2:g.43997_43998insTGT

Transcript Alleles

HGVS Amino-acid change
ENST00000248633.9:c.3637-112_3637-111insTGT (PEX1) MANE Select ENSP00000248633.4:n.3637-112_3637-111insTGT
ENST00000248633.8:c.3637-112_3637-111insTGT (PEX1) ENSP00000248633.4:n.3637-112_3637-111insTGT
ENST00000428214.5:c.3466-112_3466-111insTGT (PEX1) ENSP00000394413.1:n.3466-112_3466-111insTGT
ENST00000438045.5:c.2671-112_2671-111insTGT (PEX1) ENSP00000410438.1:n.2671-112_2671-111insTGT
ENST00000469417.1:n.534-112_534-111insTGT (PEX1)
ENST00000477342.1:n.260_261insTGT (PEX1)
ENST00000484913.5:n.3676-112_3676-111insTGT (PEX1)
ENST00000496420.5:n.4687-112_4687-111insTGT (PEX1)
NM_000466.2:c.3637-112_3637-111insTGT (PEX1) NP_000457.1:n.3637-112_3637-111insTGT
NM_001282677.1:c.3466-112_3466-111insTGT (PEX1) NP_001269606.1:n.3466-112_3466-111insTGT
NM_001282678.1:c.3013-112_3013-111insTGT (PEX1) NP_001269607.1:n.3013-112_3013-111insTGT
XM_005250433.3:c.1888-112_1888-111insTGT (PEX1) XP_005250490.1:n.1888-112_1888-111insTGT
XR_242246.3:n.3728-112_3728-111insTGT (PEX1)
XR_927494.1:n.1036-1709_1036-1708insACA (GATAD1)
XR_927495.1:n.1036-552_1036-551insACA (GATAD1)
XR_927496.1:n.1041-1709_1041-1708insACA (GATAD1)
XR_927497.1:n.1036-552_1036-551insACA (GATAD1)
XR_927498.1:n.1124-1709_1124-1708insACA (GATAD1)
XR_927500.1:n.1033-1709_1033-1708insACA (GATAD1)
XR_927502.1:n.1033-552_1033-551insACA (GATAD1)
XR_927503.1:n.967-1709_967-1708insACA (GATAD1)
XM_017012319.2:c.1888-112_1888-111insTGT (PEX1) XP_016867808.1:n.1888-112_1888-111insTGT
XR_001744808.2:n.2659-112_2659-111insTGT (PEX1)
XR_001744842.2:n.2281-1709_2281-1708insACA (GATAD1)
XR_001744843.2:n.2212-1709_2212-1708insACA (GATAD1)
XR_002956472.1:n.2281-552_2281-551insACA (GATAD1)
XR_002956473.1:n.2369-1709_2369-1708insACA (GATAD1)
XR_002956474.1:n.2286-1709_2286-1708insACA (GATAD1)
XR_242246.5:n.3679-112_3679-111insTGT (PEX1)
XR_927494.3:n.1063-1709_1063-1708insACA (GATAD1)
XR_927500.3:n.1060-1709_1060-1708insACA (GATAD1)
XR_927503.3:n.994-1709_994-1708insACA (GATAD1)
NM_000466.3:c.3637-112_3637-111insTGT (PEX1) MANE Select NP_000457.1:n.3637-112_3637-111insTGT
NM_001282677.2:c.3466-112_3466-111insTGT (PEX1) NP_001269606.1:n.3466-112_3466-111insTGT
NM_001282678.2:c.3013-112_3013-111insTGT (PEX1) NP_001269607.1:n.3013-112_3013-111insTGT