Canonical Allele Identifier: CA368164635

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92491458C>A , CM000669.2:g.92491458C>A GRCh38
NC_000007.13:g.92120772C>A , CM000669.1:g.92120772C>A GRCh37
NC_000007.12:g.91958708C>A NCBI36
NG_008341.1:g.42074G>T
NG_008341.2:g.42074G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.3252G>T (PEX1) MANE Select ENSP00000248633.4:p.Met1084Ile
ENST00000248633.8:c.3252G>T (PEX1) ENSP00000248633.4:p.Met1084Ile
ENST00000428214.5:c.3081G>T (PEX1) ENSP00000394413.1:p.Met1027Ile
ENST00000438045.5:c.2286G>T (PEX1) ENSP00000410438.1:p.Met762Ile
ENST00000484913.5:n.3291G>T (PEX1)
ENST00000496420.5:n.4307G>T (PEX1)
NM_000466.2:c.3252G>T (PEX1) NP_000457.1:p.Met1084Ile
NM_001282677.1:c.3081G>T (PEX1) NP_001269606.1:p.Met1027Ile
NM_001282678.1:c.2628G>T (PEX1) NP_001269607.1:p.Met876Ile
XM_005250433.3:c.1503G>T (PEX1) XP_005250490.1:p.Met501Ile
XR_242246.3:n.3348G>T (PEX1)
XM_017012319.2:c.1503G>T (PEX1) XP_016867808.1:p.Met501Ile
XR_001744808.2:n.2279G>T (PEX1)
XR_001744842.2:n.2496C>A (GATAD1)
XR_001744843.2:n.2427C>A (GATAD1)
XR_002956472.1:n.2553C>A (GATAD1)
XR_002956473.1:n.2584C>A (GATAD1)
XR_002956474.1:n.2501C>A (GATAD1)
XR_242246.5:n.3299G>T (PEX1)
XR_927494.3:n.1278C>A (GATAD1)
XR_927500.3:n.1275C>A (GATAD1)
XR_927503.3:n.1209C>A (GATAD1)
NM_000466.3:c.3252G>T (PEX1) MANE Select NP_000457.1:p.Met1084Ile
NM_001282677.2:c.3081G>T (PEX1) NP_001269606.1:p.Met1027Ile
NM_001282678.2:c.2628G>T (PEX1) NP_001269607.1:p.Met876Ile