Canonical Allele Identifier: CA2683717918

Linked Data

gnomAD v4: 7-92494206-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92494206C>T , CM000669.2:g.92494206C>T GRCh38
NC_000007.13:g.92123520C>T , CM000669.1:g.92123520C>T GRCh37
NC_000007.12:g.91961456C>T NCBI36
NG_008341.1:g.39326G>A
NG_008341.2:g.39326G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.3030+87G>A (PEX1) MANE Select ENSP00000248633.4:n.3030+87G>A
ENST00000248633.8:c.3030+87G>A (PEX1) ENSP00000248633.4:n.3030+87G>A
ENST00000428214.5:c.2859+87G>A (PEX1) ENSP00000394413.1:n.2859+87G>A
ENST00000438045.5:c.2064+87G>A (PEX1) ENSP00000410438.1:n.2064+87G>A
ENST00000484913.5:n.3069+87G>A (PEX1)
ENST00000496420.5:n.3009G>A (PEX1)
NM_000466.2:c.3030+87G>A (PEX1) NP_000457.1:n.3030+87G>A
NM_001282677.1:c.2859+87G>A (PEX1) NP_001269606.1:n.2859+87G>A
NM_001282678.1:c.2406+87G>A (PEX1) NP_001269607.1:n.2406+87G>A
XM_005250433.3:c.1281+87G>A (PEX1) XP_005250490.1:n.1281+87G>A
XR_242246.3:n.3126+87G>A (PEX1)
XM_017012319.2:c.1281+87G>A (PEX1) XP_016867808.1:n.1281+87G>A
XR_001744808.2:n.2057+87G>A (PEX1)
XR_001744843.2:n.5175C>T (GATAD1)
XR_242246.5:n.3077+87G>A (PEX1)
XR_927494.3:n.4026C>T (GATAD1)
XR_927503.3:n.3957C>T (GATAD1)
NM_000466.3:c.3030+87G>A (PEX1) MANE Select NP_000457.1:n.3030+87G>A
NM_001282677.2:c.2859+87G>A (PEX1) NP_001269606.1:n.2859+87G>A
NM_001282678.2:c.2406+87G>A (PEX1) NP_001269607.1:n.2406+87G>A