Canonical Allele Identifier: CA456624146

Linked Data

MyVariant Identifiers: chr7:g.92120730T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92491416T>A , CM000669.2:g.92491416T>A GRCh38
NC_000007.13:g.92120730T>A , CM000669.1:g.92120730T>A GRCh37
NC_000007.12:g.91958666T>A NCBI36
NG_008341.1:g.42116A>T
NG_008341.2:g.42116A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000248633.9:c.3294A>T (PEX1) MANE Select ENSP00000248633.4:p.Gly1098=
ENST00000248633.8:c.3294A>T (PEX1) ENSP00000248633.4:p.Gly1098=
ENST00000428214.5:c.3123A>T (PEX1) ENSP00000394413.1:p.Gly1041=
ENST00000438045.5:c.2328A>T (PEX1) ENSP00000410438.1:p.Gly776=
ENST00000484913.5:n.3333A>T (PEX1)
ENST00000496420.5:n.4349A>T (PEX1)
NM_000466.2:c.3294A>T (PEX1) NP_000457.1:p.Gly1098=
NM_001282677.1:c.3123A>T (PEX1) NP_001269606.1:p.Gly1041=
NM_001282678.1:c.2670A>T (PEX1) NP_001269607.1:p.Gly890=
XM_005250433.3:c.1545A>T (PEX1) XP_005250490.1:p.Gly515=
XR_242246.3:n.3390A>T (PEX1)
XM_017012319.2:c.1545A>T (PEX1) XP_016867808.1:p.Gly515=
XR_001744808.2:n.2321A>T (PEX1)
XR_001744842.2:n.2454T>A (GATAD1)
XR_001744843.2:n.2385T>A (GATAD1)
XR_002956472.1:n.2511T>A (GATAD1)
XR_002956473.1:n.2542T>A (GATAD1)
XR_002956474.1:n.2459T>A (GATAD1)
XR_242246.5:n.3341A>T (PEX1)
XR_927494.3:n.1236T>A (GATAD1)
XR_927500.3:n.1233T>A (GATAD1)
XR_927503.3:n.1167T>A (GATAD1)
NM_000466.3:c.3294A>T (PEX1) MANE Select NP_000457.1:p.Gly1098=
NM_001282677.2:c.3123A>T (PEX1) NP_001269606.1:p.Gly1041=
NM_001282678.2:c.2670A>T (PEX1) NP_001269607.1:p.Gly890=