Canonical Allele Identifier: CA368185103

Gene: PEX1

Linked Data

• ClinVar Variation Id: 1725090
• ClinVar RCV Id: RCV002308149
• MyVariant Identifiers: chr7:g.92135622T>A (hg19) ; chr7:g.92506308T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92506308T>A , CM000669.2:g.92506308T>A	GRCh38
NC_000007.13:g.92135622T>A , CM000669.1:g.92135622T>A	GRCh37
NC_000007.12:g.91973558T>A	NCBI36
NG_008341.1:g.27224A>T
NG_008341.2:g.27224A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000248633.9:c.1840A>T MANE Select	ENSP00000248633.4:p.Lys614Ter
ENST00000248633.8:c.1840A>T	ENSP00000248633.4:p.Lys614Ter
ENST00000422866.1:c.658A>T
ENST00000428214.5:c.1840A>T	ENSP00000394413.1:p.Lys614Ter
ENST00000438045.5:c.874A>T	ENSP00000410438.1:p.Lys292Ter
ENST00000484913.5:n.1879A>T
ENST00000496420.5:n.1516A>T
NM_000466.2:c.1840A>T	NP_000457.1:p.Lys614Ter
NM_001282677.1:c.1840A>T	NP_001269606.1:p.Lys614Ter
NM_001282678.1:c.1216A>T	NP_001269607.1:p.Lys406Ter
XM_005250433.3:c.91A>T	XP_005250490.1:p.Lys31Ter
XR_242246.3:n.1936A>T
XM_017012319.2:c.91A>T	XP_016867808.1:p.Lys31Ter
XR_001744808.2:n.867A>T
XR_242246.5:n.1887A>T
NM_000466.3:c.1840A>T MANE Select	NP_000457.1:p.Lys614Ter
NM_001282677.2:c.1840A>T	NP_001269606.1:p.Lys614Ter
NM_001282678.2:c.1216A>T	NP_001269607.1:p.Lys406Ter