Canonical Allele Identifier: CA368188665

Gene: PEX1

Linked Data

• ClinVar Variation Id: 2677614
• ClinVar RCV Id: RCV003476748
• MyVariant Identifiers: chr7:g.92140257C>G (hg19) ; chr7:g.92510943C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92510943C>G , CM000669.2:g.92510943C>G	GRCh38
NC_000007.13:g.92140257C>G , CM000669.1:g.92140257C>G	GRCh37
NC_000007.12:g.91978193C>G	NCBI36
NG_008341.1:g.22589G>C
NG_008341.2:g.22589G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000248633.9:c.1587+1G>C MANE Select	ENSP00000248633.4:n.1587+1G>C
ENST00000248633.8:c.1587+1G>C	ENSP00000248633.4:n.1587+1G>C
ENST00000422866.1:c.488+1G>C
ENST00000428214.5:c.1587+1G>C	ENSP00000394413.1:n.1587+1G>C
ENST00000438045.5:c.621+1G>C	ENSP00000410438.1:n.621+1G>C
ENST00000476923.1:n.349G>C
ENST00000484913.5:n.1626+1G>C
NM_000466.2:c.1587+1G>C	NP_000457.1:n.1587+1G>C
NM_001282677.1:c.1587+1G>C	NP_001269606.1:n.1587+1G>C
NM_001282678.1:c.963+1G>C	NP_001269607.1:n.963+1G>C
XM_005250433.3:c.-80+1G>C	XP_005250490.1:n.-80+1G>C
XR_242246.3:n.1683+1G>C
XM_017012319.2:c.-80+1G>C	XP_016867808.1:n.-80+1G>C
XR_001744808.2:n.697+1G>C
XR_242246.5:n.1634+1G>C
NM_000466.3:c.1587+1G>C MANE Select	NP_000457.1:n.1587+1G>C
NM_001282677.2:c.1587+1G>C	NP_001269606.1:n.1587+1G>C
NM_001282678.2:c.963+1G>C	NP_001269607.1:n.963+1G>C