Canonical Allele Identifier: CA1725951650
Gene: PEX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92522125_92522126delinsGT , CM000669.2:g.92522125_92522126delinsGT GRCh38
NC_000007.13:g.92151439_92151440delinsGT , CM000669.1:g.92151439_92151440delinsGT GRCh37
NC_000007.12:g.91989375_91989376delinsGT NCBI36
NG_008341.1:g.11406_11407delinsAC
NG_008341.2:g.11406_11407delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.249_250delinsAC MANE Select ENSP00000248633.4:p.Lys83=
ENST00000248633.8:c.249_250delinsAC ENSP00000248633.4:p.Lys83=
ENST00000428214.5:c.249_250delinsAC ENSP00000394413.1:p.Lys83=
ENST00000438045.5:c.249_250delinsAC ENSP00000410438.1:p.Lys83=
ENST00000484913.5:n.253_254delinsAC
NM_000466.2:c.249_250delinsAC NP_000457.1:p.Lys83=
NM_001282677.1:c.249_250delinsAC NP_001269606.1:p.Lys83=
NM_001282678.1:c.-411_-410delinsAC NP_001269607.1:n.-411_-410delinsAC
XR_242246.3:n.345_346delinsAC
XR_242246.5:n.296_297delinsAC
NM_000466.3:c.249_250delinsAC MANE Select NP_000457.1:p.Lys83=
NM_001282677.2:c.249_250delinsAC NP_001269606.1:p.Lys83=
NM_001282678.2:c.-411_-410delinsAC NP_001269607.1:n.-411_-410delinsAC