Canonical Allele Identifier: CA368168046

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92494486C>A , CM000669.2:g.92494486C>A GRCh38
NC_000007.13:g.92123800C>A , CM000669.1:g.92123800C>A GRCh37
NC_000007.12:g.91961736C>A NCBI36
NG_008341.1:g.39046G>T
NG_008341.2:g.39046G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.2926+1G>T (PEX1) MANE Select ENSP00000248633.4:n.2926+1G>T
ENST00000248633.8:c.2926+1G>T (PEX1) ENSP00000248633.4:n.2926+1G>T
ENST00000428214.5:c.2755+1G>T (PEX1) ENSP00000394413.1:n.2755+1G>T
ENST00000438045.5:c.1960+1G>T (PEX1) ENSP00000410438.1:n.1960+1G>T
ENST00000484913.5:n.2965+1G>T (PEX1)
ENST00000496420.5:n.2818+1G>T (PEX1)
NM_000466.2:c.2926+1G>T (PEX1) NP_000457.1:n.2926+1G>T
NM_001282677.1:c.2755+1G>T (PEX1) NP_001269606.1:n.2755+1G>T
NM_001282678.1:c.2302+1G>T (PEX1) NP_001269607.1:n.2302+1G>T
XM_005250433.3:c.1177+1G>T (PEX1) XP_005250490.1:n.1177+1G>T
XR_242246.3:n.3022+1G>T (PEX1)
XM_017012319.2:c.1177+1G>T (PEX1) XP_016867808.1:n.1177+1G>T
XR_001744808.2:n.1953+1G>T (PEX1)
XR_001744843.2:n.5455C>A (GATAD1)
XR_242246.5:n.2973+1G>T (PEX1)
XR_927494.3:n.4306C>A (GATAD1)
XR_927503.3:n.4237C>A (GATAD1)
NM_000466.3:c.2926+1G>T (PEX1) MANE Select NP_000457.1:n.2926+1G>T
NM_001282677.2:c.2755+1G>T (PEX1) NP_001269606.1:n.2755+1G>T
NM_001282678.2:c.2302+1G>T (PEX1) NP_001269607.1:n.2302+1G>T