Canonical Allele Identifier: CA368198037
Gene: PEX1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92517410T>A , CM000669.2:g.92517410T>A GRCh38
NC_000007.13:g.92146724T>A , CM000669.1:g.92146724T>A GRCh37
NC_000007.12:g.91984660T>A NCBI36
NG_008341.1:g.16122A>T
NG_008341.2:g.16122A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.1105A>T MANE Select ENSP00000248633.4:p.Lys369Ter
ENST00000248633.8:c.1105A>T ENSP00000248633.4:p.Lys369Ter
ENST00000422866.1:c.6A>T
ENST00000428214.5:c.1105A>T ENSP00000394413.1:p.Lys369Ter
ENST00000438045.5:c.274-3443A>T ENSP00000410438.1:n.274-3443A>T
ENST00000484913.5:n.1144A>T
NM_000466.2:c.1105A>T NP_000457.1:p.Lys369Ter
NM_001282677.1:c.1105A>T NP_001269606.1:p.Lys369Ter
NM_001282678.1:c.481A>T NP_001269607.1:p.Lys161Ter
XR_242246.3:n.1201A>T
XM_017012319.2:c.-562A>T XP_016867808.1:n.-562A>T
XR_001744808.2:n.215A>T
XR_242246.5:n.1152A>T
NM_000466.3:c.1105A>T MANE Select NP_000457.1:p.Lys369Ter
NM_001282677.2:c.1105A>T NP_001269606.1:p.Lys369Ter
NM_001282678.2:c.481A>T NP_001269607.1:p.Lys161Ter