Canonical Allele Identifier: CA456624358

Linked Data

MyVariant Identifiers: chr7:g.92120799A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92491485A>C , CM000669.2:g.92491485A>C GRCh38
NC_000007.13:g.92120799A>C , CM000669.1:g.92120799A>C GRCh37
NC_000007.12:g.91958735A>C NCBI36
NG_008341.1:g.42047T>G
NG_008341.2:g.42047T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.3225T>G (PEX1) MANE Select ENSP00000248633.4:p.Ser1075=
ENST00000248633.8:c.3225T>G (PEX1) ENSP00000248633.4:p.Ser1075=
ENST00000428214.5:c.3054T>G (PEX1) ENSP00000394413.1:p.Ser1018=
ENST00000438045.5:c.2259T>G (PEX1) ENSP00000410438.1:p.Ser753=
ENST00000484913.5:n.3264T>G (PEX1)
ENST00000496420.5:n.4280T>G (PEX1)
NM_000466.2:c.3225T>G (PEX1) NP_000457.1:p.Ser1075=
NM_001282677.1:c.3054T>G (PEX1) NP_001269606.1:p.Ser1018=
NM_001282678.1:c.2601T>G (PEX1) NP_001269607.1:p.Ser867=
XM_005250433.3:c.1476T>G (PEX1) XP_005250490.1:p.Ser492=
XR_242246.3:n.3321T>G (PEX1)
XM_017012319.2:c.1476T>G (PEX1) XP_016867808.1:p.Ser492=
XR_001744808.2:n.2252T>G (PEX1)
XR_001744842.2:n.2523A>C (GATAD1)
XR_001744843.2:n.2454A>C (GATAD1)
XR_002956472.1:n.2580A>C (GATAD1)
XR_002956473.1:n.2611A>C (GATAD1)
XR_002956474.1:n.2528A>C (GATAD1)
XR_242246.5:n.3272T>G (PEX1)
XR_927494.3:n.1305A>C (GATAD1)
XR_927500.3:n.1302A>C (GATAD1)
XR_927503.3:n.1236A>C (GATAD1)
NM_000466.3:c.3225T>G (PEX1) MANE Select NP_000457.1:p.Ser1075=
NM_001282677.2:c.3054T>G (PEX1) NP_001269606.1:p.Ser1018=
NM_001282678.2:c.2601T>G (PEX1) NP_001269607.1:p.Ser867=