Canonical Allele Identifier: CA2522566265
Gene: PEX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92506398T>A , CM000669.2:g.92506398T>A GRCh38
NC_000007.13:g.92135712T>A , CM000669.1:g.92135712T>A GRCh37
NC_000007.12:g.91973648T>A NCBI36
NG_008341.1:g.27134A>T
NG_008341.2:g.27134A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.1804-54A>T MANE Select ENSP00000248633.4:n.1804-54A>T
ENST00000248633.8:c.1804-54A>T ENSP00000248633.4:n.1804-54A>T
ENST00000422866.1:c.622-54A>T
ENST00000428214.5:c.1804-54A>T ENSP00000394413.1:n.1804-54A>T
ENST00000438045.5:c.838-54A>T ENSP00000410438.1:n.838-54A>T
ENST00000484913.5:n.1843-54A>T
ENST00000496420.5:n.1426A>T
NM_000466.2:c.1804-54A>T NP_000457.1:n.1804-54A>T
NM_001282677.1:c.1804-54A>T NP_001269606.1:n.1804-54A>T
NM_001282678.1:c.1180-54A>T NP_001269607.1:n.1180-54A>T
XM_005250433.3:c.55-54A>T XP_005250490.1:n.55-54A>T
XR_242246.3:n.1900-54A>T
XM_017012319.2:c.55-54A>T XP_016867808.1:n.55-54A>T
XR_001744808.2:n.831-54A>T
XR_242246.5:n.1851-54A>T
NM_000466.3:c.1804-54A>T MANE Select NP_000457.1:n.1804-54A>T
NM_001282677.2:c.1804-54A>T NP_001269606.1:n.1804-54A>T
NM_001282678.2:c.1180-54A>T NP_001269607.1:n.1180-54A>T