Canonical Allele Identifier: CA2683717854

Linked Data

gnomAD v4: 7-92494105-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92494105C>G , CM000669.2:g.92494105C>G GRCh38
NC_000007.13:g.92123419C>G , CM000669.1:g.92123419C>G GRCh37
NC_000007.12:g.91961355C>G NCBI36
NG_008341.1:g.39427G>C
NG_008341.2:g.39427G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.3030+188G>C (PEX1) MANE Select ENSP00000248633.4:n.3030+188G>C
ENST00000248633.8:c.3030+188G>C (PEX1) ENSP00000248633.4:n.3030+188G>C
ENST00000428214.5:c.2859+188G>C (PEX1) ENSP00000394413.1:n.2859+188G>C
ENST00000438045.5:c.2064+188G>C (PEX1) ENSP00000410438.1:n.2064+188G>C
ENST00000484913.5:n.3069+188G>C (PEX1)
ENST00000496420.5:n.3110G>C (PEX1)
NM_000466.2:c.3030+188G>C (PEX1) NP_000457.1:n.3030+188G>C
NM_001282677.1:c.2859+188G>C (PEX1) NP_001269606.1:n.2859+188G>C
NM_001282678.1:c.2406+188G>C (PEX1) NP_001269607.1:n.2406+188G>C
XM_005250433.3:c.1281+188G>C (PEX1) XP_005250490.1:n.1281+188G>C
XR_242246.3:n.3126+188G>C (PEX1)
XM_017012319.2:c.1281+188G>C (PEX1) XP_016867808.1:n.1281+188G>C
XR_001744808.2:n.2057+188G>C (PEX1)
XR_001744843.2:n.5074C>G (GATAD1)
XR_242246.5:n.3077+188G>C (PEX1)
XR_927494.3:n.3925C>G (GATAD1)
XR_927503.3:n.3856C>G (GATAD1)
NM_000466.3:c.3030+188G>C (PEX1) MANE Select NP_000457.1:n.3030+188G>C
NM_001282677.2:c.2859+188G>C (PEX1) NP_001269606.1:n.2859+188G>C
NM_001282678.2:c.2406+188G>C (PEX1) NP_001269607.1:n.2406+188G>C