Canonical Allele Identifier: CA1725926720

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92489499_92489502delinsCTTA , CM000669.2:g.92489499_92489502delinsCTTA GRCh38
NC_000007.13:g.92118813_92118816delinsCTTA , CM000669.1:g.92118813_92118816delinsCTTA GRCh37
NC_000007.12:g.91956749_91956752delinsCTTA NCBI36
NG_008341.1:g.44030_44033delinsTAAG
NG_008341.2:g.44030_44033delinsTAAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.3637-79_3637-76delinsTAAG (PEX1) MANE Select ENSP00000248633.4:n.3637-79_3637-76delinsTAAG
ENST00000248633.8:c.3637-79_3637-76delinsTAAG (PEX1) ENSP00000248633.4:n.3637-79_3637-76delinsTAAG
ENST00000428214.5:c.3466-79_3466-76delinsTAAG (PEX1) ENSP00000394413.1:n.3466-79_3466-76delinsTAAG
ENST00000438045.5:c.2671-79_2671-76delinsTAAG (PEX1) ENSP00000410438.1:n.2671-79_2671-76delinsTAAG
ENST00000469417.1:n.534-79_534-76delinsTAAG (PEX1)
ENST00000477342.1:n.293_296delinsTAAG (PEX1)
ENST00000484913.5:n.3676-79_3676-76delinsTAAG (PEX1)
ENST00000496420.5:n.4687-79_4687-76delinsTAAG (PEX1)
NM_000466.2:c.3637-79_3637-76delinsTAAG (PEX1) NP_000457.1:n.3637-79_3637-76delinsTAAG
NM_001282677.1:c.3466-79_3466-76delinsTAAG (PEX1) NP_001269606.1:n.3466-79_3466-76delinsTAAG
NM_001282678.1:c.3013-79_3013-76delinsTAAG (PEX1) NP_001269607.1:n.3013-79_3013-76delinsTAAG
XM_005250433.3:c.1888-79_1888-76delinsTAAG (PEX1) XP_005250490.1:n.1888-79_1888-76delinsTAAG
XR_242246.3:n.3728-79_3728-76delinsTAAG (PEX1)
XR_927494.1:n.1036-1744_1036-1741delinsCTTA (GATAD1)
XR_927495.1:n.1036-587_1036-584delinsCTTA (GATAD1)
XR_927496.1:n.1041-1744_1041-1741delinsCTTA (GATAD1)
XR_927497.1:n.1036-587_1036-584delinsCTTA (GATAD1)
XR_927498.1:n.1124-1744_1124-1741delinsCTTA (GATAD1)
XR_927500.1:n.1033-1744_1033-1741delinsCTTA (GATAD1)
XR_927502.1:n.1033-587_1033-584delinsCTTA (GATAD1)
XR_927503.1:n.967-1744_967-1741delinsCTTA (GATAD1)
XM_017012319.2:c.1888-79_1888-76delinsTAAG (PEX1) XP_016867808.1:n.1888-79_1888-76delinsTAAG
XR_001744808.2:n.2659-79_2659-76delinsTAAG (PEX1)
XR_001744842.2:n.2281-1744_2281-1741delinsCTTA (GATAD1)
XR_001744843.2:n.2212-1744_2212-1741delinsCTTA (GATAD1)
XR_002956472.1:n.2281-587_2281-584delinsCTTA (GATAD1)
XR_002956473.1:n.2369-1744_2369-1741delinsCTTA (GATAD1)
XR_002956474.1:n.2286-1744_2286-1741delinsCTTA (GATAD1)
XR_242246.5:n.3679-79_3679-76delinsTAAG (PEX1)
XR_927494.3:n.1063-1744_1063-1741delinsCTTA (GATAD1)
XR_927500.3:n.1060-1744_1060-1741delinsCTTA (GATAD1)
XR_927503.3:n.994-1744_994-1741delinsCTTA (GATAD1)
NM_000466.3:c.3637-79_3637-76delinsTAAG (PEX1) MANE Select NP_000457.1:n.3637-79_3637-76delinsTAAG
NM_001282677.2:c.3466-79_3466-76delinsTAAG (PEX1) NP_001269606.1:n.3466-79_3466-76delinsTAAG
NM_001282678.2:c.3013-79_3013-76delinsTAAG (PEX1) NP_001269607.1:n.3013-79_3013-76delinsTAAG