Canonical Allele Identifier: CA368168176

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92494496C>G , CM000669.2:g.92494496C>G GRCh38
NC_000007.13:g.92123810C>G , CM000669.1:g.92123810C>G GRCh37
NC_000007.12:g.91961746C>G NCBI36
NG_008341.1:g.39036G>C
NG_008341.2:g.39036G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.2917G>C (PEX1) MANE Select ENSP00000248633.4:p.Gly973Arg
ENST00000248633.8:c.2917G>C (PEX1) ENSP00000248633.4:p.Gly973Arg
ENST00000428214.5:c.2746G>C (PEX1) ENSP00000394413.1:p.Gly916Arg
ENST00000438045.5:c.1951G>C (PEX1) ENSP00000410438.1:p.Gly651Arg
ENST00000484913.5:n.2956G>C (PEX1)
ENST00000496420.5:n.2809G>C (PEX1)
NM_000466.2:c.2917G>C (PEX1) NP_000457.1:p.Gly973Arg
NM_001282677.1:c.2746G>C (PEX1) NP_001269606.1:p.Gly916Arg
NM_001282678.1:c.2293G>C (PEX1) NP_001269607.1:p.Gly765Arg
XM_005250433.3:c.1168G>C (PEX1) XP_005250490.1:p.Gly390Arg
XR_242246.3:n.3013G>C (PEX1)
XM_017012319.2:c.1168G>C (PEX1) XP_016867808.1:p.Gly390Arg
XR_001744808.2:n.1944G>C (PEX1)
XR_001744843.2:n.5465C>G (GATAD1)
XR_242246.5:n.2964G>C (PEX1)
XR_927494.3:n.4316C>G (GATAD1)
XR_927503.3:n.4247C>G (GATAD1)
NM_000466.3:c.2917G>C (PEX1) MANE Select NP_000457.1:p.Gly973Arg
NM_001282677.2:c.2746G>C (PEX1) NP_001269606.1:p.Gly916Arg
NM_001282678.2:c.2293G>C (PEX1) NP_001269607.1:p.Gly765Arg