Canonical Allele Identifier: CA2683717973

Linked Data

gnomAD v4: 7-92494464-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92494464A>T , CM000669.2:g.92494464A>T GRCh38
NC_000007.13:g.92123778A>T , CM000669.1:g.92123778A>T GRCh37
NC_000007.12:g.91961714A>T NCBI36
NG_008341.1:g.39068T>A
NG_008341.2:g.39068T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.2926+23T>A (PEX1) MANE Select ENSP00000248633.4:n.2926+23T>A
ENST00000248633.8:c.2926+23T>A (PEX1) ENSP00000248633.4:n.2926+23T>A
ENST00000428214.5:c.2755+23T>A (PEX1) ENSP00000394413.1:n.2755+23T>A
ENST00000438045.5:c.1960+23T>A (PEX1) ENSP00000410438.1:n.1960+23T>A
ENST00000484913.5:n.2965+23T>A (PEX1)
ENST00000496420.5:n.2818+23T>A (PEX1)
NM_000466.2:c.2926+23T>A (PEX1) NP_000457.1:n.2926+23T>A
NM_001282677.1:c.2755+23T>A (PEX1) NP_001269606.1:n.2755+23T>A
NM_001282678.1:c.2302+23T>A (PEX1) NP_001269607.1:n.2302+23T>A
XM_005250433.3:c.1177+23T>A (PEX1) XP_005250490.1:n.1177+23T>A
XR_242246.3:n.3022+23T>A (PEX1)
XM_017012319.2:c.1177+23T>A (PEX1) XP_016867808.1:n.1177+23T>A
XR_001744808.2:n.1953+23T>A (PEX1)
XR_001744843.2:n.5433A>T (GATAD1)
XR_242246.5:n.2973+23T>A (PEX1)
XR_927494.3:n.4284A>T (GATAD1)
XR_927503.3:n.4215A>T (GATAD1)
NM_000466.3:c.2926+23T>A (PEX1) MANE Select NP_000457.1:n.2926+23T>A
NM_001282677.2:c.2755+23T>A (PEX1) NP_001269606.1:n.2755+23T>A
NM_001282678.2:c.2302+23T>A (PEX1) NP_001269607.1:n.2302+23T>A