Canonical Allele Identifier: CA456624457
Gene: PEX1 HGNC NCBI

Linked Data

gnomAD v4: 7-92517843-T-G
MyVariant Identifiers: chr7:g.92147157T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92517843T>G , CM000669.2:g.92517843T>G GRCh38
NC_000007.13:g.92147157T>G , CM000669.1:g.92147157T>G GRCh37
NC_000007.12:g.91985093T>G NCBI36
NG_008341.1:g.15689A>C
NG_008341.2:g.15689A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.672A>C MANE Select ENSP00000248633.4:p.Gly224=
ENST00000248633.8:c.672A>C ENSP00000248633.4:p.Gly224=
ENST00000428214.5:c.672A>C ENSP00000394413.1:p.Gly224=
ENST00000438045.5:c.274-3876A>C ENSP00000410438.1:n.274-3876A>C
ENST00000484913.5:n.711A>C
NM_000466.2:c.672A>C NP_000457.1:p.Gly224=
NM_001282677.1:c.672A>C NP_001269606.1:p.Gly224=
NM_001282678.1:c.48A>C NP_001269607.1:p.Gly16=
XR_242246.3:n.768A>C
XR_242246.5:n.719A>C
NM_000466.3:c.672A>C MANE Select NP_000457.1:p.Gly224=
NM_001282677.2:c.672A>C NP_001269606.1:p.Gly224=
NM_001282678.2:c.48A>C NP_001269607.1:p.Gly16=