Canonical Allele Identifier: CA1725948500
Gene: PEX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92518181A= , CM000669.2:g.92518181A= GRCh38
NC_000007.13:g.92147495A= , CM000669.1:g.92147495A= GRCh37
NC_000007.12:g.91985431A= NCBI36
NG_008341.1:g.15351T=
NG_008341.2:g.15351T=

Transcript Alleles

HGVS Amino-acid change
ENST00000248633.9:c.432T= MANE Select ENSP00000248633.4:p.Pro144=
ENST00000248633.8:c.432T= ENSP00000248633.4:p.Pro144=
ENST00000428214.5:c.432T= ENSP00000394413.1:p.Pro144=
ENST00000438045.5:c.273+3921T= ENSP00000410438.1:n.273+3921T=
ENST00000484913.5:n.471T=
NM_000466.2:c.432T= NP_000457.1:p.Pro144=
NM_001282677.1:c.432T= NP_001269606.1:p.Pro144=
NM_001282678.1:c.-193T= NP_001269607.1:n.-193T=
XR_242246.3:n.528T=
XR_242246.5:n.479T=
NM_000466.3:c.432T= MANE Select NP_000457.1:p.Pro144=
NM_001282677.2:c.432T= NP_001269606.1:p.Pro144=
NM_001282678.2:c.-193T= NP_001269607.1:n.-193T=