Canonical Allele Identifier: CA2683717974

Linked Data

gnomAD v4: 7-92494469-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92494469T>C , CM000669.2:g.92494469T>C GRCh38
NC_000007.13:g.92123783T>C , CM000669.1:g.92123783T>C GRCh37
NC_000007.12:g.91961719T>C NCBI36
NG_008341.1:g.39063A>G
NG_008341.2:g.39063A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.2926+18A>G (PEX1) MANE Select ENSP00000248633.4:n.2926+18A>G
ENST00000248633.8:c.2926+18A>G (PEX1) ENSP00000248633.4:n.2926+18A>G
ENST00000428214.5:c.2755+18A>G (PEX1) ENSP00000394413.1:n.2755+18A>G
ENST00000438045.5:c.1960+18A>G (PEX1) ENSP00000410438.1:n.1960+18A>G
ENST00000484913.5:n.2965+18A>G (PEX1)
ENST00000496420.5:n.2818+18A>G (PEX1)
NM_000466.2:c.2926+18A>G (PEX1) NP_000457.1:n.2926+18A>G
NM_001282677.1:c.2755+18A>G (PEX1) NP_001269606.1:n.2755+18A>G
NM_001282678.1:c.2302+18A>G (PEX1) NP_001269607.1:n.2302+18A>G
XM_005250433.3:c.1177+18A>G (PEX1) XP_005250490.1:n.1177+18A>G
XR_242246.3:n.3022+18A>G (PEX1)
XM_017012319.2:c.1177+18A>G (PEX1) XP_016867808.1:n.1177+18A>G
XR_001744808.2:n.1953+18A>G (PEX1)
XR_001744843.2:n.5438T>C (GATAD1)
XR_242246.5:n.2973+18A>G (PEX1)
XR_927494.3:n.4289T>C (GATAD1)
XR_927503.3:n.4220T>C (GATAD1)
NM_000466.3:c.2926+18A>G (PEX1) MANE Select NP_000457.1:n.2926+18A>G
NM_001282677.2:c.2755+18A>G (PEX1) NP_001269606.1:n.2755+18A>G
NM_001282678.2:c.2302+18A>G (PEX1) NP_001269607.1:n.2302+18A>G