Canonical Allele Identifier: CA368199239

Gene: PEX1

Linked Data

• ClinVar Variation Id: 2124180
• ClinVar RCV Id: RCV003057032
• MyVariant Identifiers: chr7:g.92146948G>C (hg19) ; chr7:g.92517634G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92517634G>C , CM000669.2:g.92517634G>C	GRCh38
NC_000007.13:g.92146948G>C , CM000669.1:g.92146948G>C	GRCh37
NC_000007.12:g.91984884G>C	NCBI36
NG_008341.1:g.15898C>G
NG_008341.2:g.15898C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.881C>G MANE Select	ENSP00000248633.4:p.Pro294Arg
ENST00000248633.8:c.881C>G	ENSP00000248633.4:p.Pro294Arg
ENST00000428214.5:c.881C>G	ENSP00000394413.1:p.Pro294Arg
ENST00000438045.5:c.274-3667C>G	ENSP00000410438.1:n.274-3667C>G
ENST00000484913.5:n.920C>G
NM_000466.2:c.881C>G	NP_000457.1:p.Pro294Arg
NM_001282677.1:c.881C>G	NP_001269606.1:p.Pro294Arg
NM_001282678.1:c.257C>G	NP_001269607.1:p.Pro86Arg
XR_242246.3:n.977C>G
XR_242246.5:n.928C>G
NM_000466.3:c.881C>G MANE Select	NP_000457.1:p.Pro294Arg
NM_001282677.2:c.881C>G	NP_001269606.1:p.Pro294Arg
NM_001282678.2:c.257C>G	NP_001269607.1:p.Pro86Arg