Canonical Allele Identifier: CA456623833

Linked Data

MyVariant Identifiers: chr7:g.92120631T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92491317T>A , CM000669.2:g.92491317T>A GRCh38
NC_000007.13:g.92120631T>A , CM000669.1:g.92120631T>A GRCh37
NC_000007.12:g.91958567T>A NCBI36
NG_008341.1:g.42215A>T
NG_008341.2:g.42215A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.3393A>T (PEX1) MANE Select ENSP00000248633.4:p.Gly1131=
ENST00000248633.8:c.3393A>T (PEX1) ENSP00000248633.4:p.Gly1131=
ENST00000428214.5:c.3222A>T (PEX1) ENSP00000394413.1:p.Gly1074=
ENST00000438045.5:c.2427A>T (PEX1) ENSP00000410438.1:p.Gly809=
ENST00000484913.5:n.3432A>T (PEX1)
ENST00000496420.5:n.4448A>T (PEX1)
NM_000466.2:c.3393A>T (PEX1) NP_000457.1:p.Gly1131=
NM_001282677.1:c.3222A>T (PEX1) NP_001269606.1:p.Gly1074=
NM_001282678.1:c.2769A>T (PEX1) NP_001269607.1:p.Gly923=
XM_005250433.3:c.1644A>T (PEX1) XP_005250490.1:p.Gly548=
XR_242246.3:n.3489A>T (PEX1)
XR_927494.1:n.1110T>A (GATAD1)
XR_927496.1:n.1115T>A (GATAD1)
XR_927497.1:n.1167T>A (GATAD1)
XR_927498.1:n.1198T>A (GATAD1)
XR_927500.1:n.1107T>A (GATAD1)
XR_927503.1:n.1041T>A (GATAD1)
XM_017012319.2:c.1644A>T (PEX1) XP_016867808.1:p.Gly548=
XR_001744808.2:n.2420A>T (PEX1)
XR_001744842.2:n.2355T>A (GATAD1)
XR_001744843.2:n.2286T>A (GATAD1)
XR_002956472.1:n.2412T>A (GATAD1)
XR_002956473.1:n.2443T>A (GATAD1)
XR_002956474.1:n.2360T>A (GATAD1)
XR_242246.5:n.3440A>T (PEX1)
XR_927494.3:n.1137T>A (GATAD1)
XR_927500.3:n.1134T>A (GATAD1)
XR_927503.3:n.1068T>A (GATAD1)
NM_000466.3:c.3393A>T (PEX1) MANE Select NP_000457.1:p.Gly1131=
NM_001282677.2:c.3222A>T (PEX1) NP_001269606.1:p.Gly1074=
NM_001282678.2:c.2769A>T (PEX1) NP_001269607.1:p.Gly923=