Canonical Allele Identifier: CA456624187

Linked Data

MyVariant Identifiers: chr7:g.92120748G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92491434G>T , CM000669.2:g.92491434G>T GRCh38
NC_000007.13:g.92120748G>T , CM000669.1:g.92120748G>T GRCh37
NC_000007.12:g.91958684G>T NCBI36
NG_008341.1:g.42098C>A
NG_008341.2:g.42098C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.3276C>A (PEX1) MANE Select ENSP00000248633.4:p.Gly1092=
ENST00000248633.8:c.3276C>A (PEX1) ENSP00000248633.4:p.Gly1092=
ENST00000428214.5:c.3105C>A (PEX1) ENSP00000394413.1:p.Gly1035=
ENST00000438045.5:c.2310C>A (PEX1) ENSP00000410438.1:p.Gly770=
ENST00000484913.5:n.3315C>A (PEX1)
ENST00000496420.5:n.4331C>A (PEX1)
NM_000466.2:c.3276C>A (PEX1) NP_000457.1:p.Gly1092=
NM_001282677.1:c.3105C>A (PEX1) NP_001269606.1:p.Gly1035=
NM_001282678.1:c.2652C>A (PEX1) NP_001269607.1:p.Gly884=
XM_005250433.3:c.1527C>A (PEX1) XP_005250490.1:p.Gly509=
XR_242246.3:n.3372C>A (PEX1)
XM_017012319.2:c.1527C>A (PEX1) XP_016867808.1:p.Gly509=
XR_001744808.2:n.2303C>A (PEX1)
XR_001744842.2:n.2472G>T (GATAD1)
XR_001744843.2:n.2403G>T (GATAD1)
XR_002956472.1:n.2529G>T (GATAD1)
XR_002956473.1:n.2560G>T (GATAD1)
XR_002956474.1:n.2477G>T (GATAD1)
XR_242246.5:n.3323C>A (PEX1)
XR_927494.3:n.1254G>T (GATAD1)
XR_927500.3:n.1251G>T (GATAD1)
XR_927503.3:n.1185G>T (GATAD1)
NM_000466.3:c.3276C>A (PEX1) MANE Select NP_000457.1:p.Gly1092=
NM_001282677.2:c.3105C>A (PEX1) NP_001269606.1:p.Gly1035=
NM_001282678.2:c.2652C>A (PEX1) NP_001269607.1:p.Gly884=