Canonical Allele Identifier: CA456480822

Linked Data

MyVariant Identifiers: chr7:g.92119172A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92489858A>C , CM000669.2:g.92489858A>C GRCh38
NC_000007.13:g.92119172A>C , CM000669.1:g.92119172A>C GRCh37
NC_000007.12:g.91957108A>C NCBI36
NG_008341.1:g.43674T>G
NG_008341.2:g.43674T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.3492T>G (PEX1) MANE Select ENSP00000248633.4:p.Val1164=
ENST00000248633.8:c.3492T>G (PEX1) ENSP00000248633.4:p.Val1164=
ENST00000428214.5:c.3321T>G (PEX1) ENSP00000394413.1:p.Val1107=
ENST00000438045.5:c.2526T>G (PEX1) ENSP00000410438.1:p.Val842=
ENST00000469417.1:n.389T>G (PEX1)
ENST00000484913.5:n.3531T>G (PEX1)
ENST00000496420.5:n.4547T>G (PEX1)
NM_000466.2:c.3492T>G (PEX1) NP_000457.1:p.Val1164=
NM_001282677.1:c.3321T>G (PEX1) NP_001269606.1:p.Val1107=
NM_001282678.1:c.2868T>G (PEX1) NP_001269607.1:p.Val956=
XM_005250433.3:c.1743T>G (PEX1) XP_005250490.1:p.Val581=
XR_242246.3:n.3588T>G (PEX1)
XR_927494.1:n.1036-1385A>C (GATAD1)
XR_927495.1:n.1036-228A>C (GATAD1)
XR_927496.1:n.1041-1385A>C (GATAD1)
XR_927497.1:n.1036-228A>C (GATAD1)
XR_927498.1:n.1124-1385A>C (GATAD1)
XR_927500.1:n.1033-1385A>C (GATAD1)
XR_927502.1:n.1033-228A>C (GATAD1)
XR_927503.1:n.967-1385A>C (GATAD1)
XM_017012319.2:c.1743T>G (PEX1) XP_016867808.1:p.Val581=
XR_001744808.2:n.2519T>G (PEX1)
XR_001744842.2:n.2281-1385A>C (GATAD1)
XR_001744843.2:n.2212-1385A>C (GATAD1)
XR_002956472.1:n.2281-228A>C (GATAD1)
XR_002956473.1:n.2369-1385A>C (GATAD1)
XR_002956474.1:n.2286-1385A>C (GATAD1)
XR_242246.5:n.3539T>G (PEX1)
XR_927494.3:n.1063-1385A>C (GATAD1)
XR_927500.3:n.1060-1385A>C (GATAD1)
XR_927503.3:n.994-1385A>C (GATAD1)
NM_000466.3:c.3492T>G (PEX1) MANE Select NP_000457.1:p.Val1164=
NM_001282677.2:c.3321T>G (PEX1) NP_001269606.1:p.Val1107=
NM_001282678.2:c.2868T>G (PEX1) NP_001269607.1:p.Val956=