Canonical Allele Identifier: CA368185124

Gene: PEX1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92506310C>T , CM000669.2:g.92506310C>T	GRCh38
NC_000007.13:g.92135624C>T , CM000669.1:g.92135624C>T	GRCh37
NC_000007.12:g.91973560C>T	NCBI36
NG_008341.1:g.27222G>A
NG_008341.2:g.27222G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.1838G>A MANE Select	ENSP00000248633.4:p.Cys613Tyr
ENST00000248633.8:c.1838G>A	ENSP00000248633.4:p.Cys613Tyr
ENST00000422866.1:c.656G>A
ENST00000428214.5:c.1838G>A	ENSP00000394413.1:p.Cys613Tyr
ENST00000438045.5:c.872G>A	ENSP00000410438.1:p.Cys291Tyr
ENST00000484913.5:n.1877G>A
ENST00000496420.5:n.1514G>A
NM_000466.2:c.1838G>A	NP_000457.1:p.Cys613Tyr
NM_001282677.1:c.1838G>A	NP_001269606.1:p.Cys613Tyr
NM_001282678.1:c.1214G>A	NP_001269607.1:p.Cys405Tyr
XM_005250433.3:c.89G>A	XP_005250490.1:p.Cys30Tyr
XR_242246.3:n.1934G>A
XM_017012319.2:c.89G>A	XP_016867808.1:p.Cys30Tyr
XR_001744808.2:n.865G>A
XR_242246.5:n.1885G>A
NM_000466.3:c.1838G>A MANE Select	NP_000457.1:p.Cys613Tyr
NM_001282677.2:c.1838G>A	NP_001269606.1:p.Cys613Tyr
NM_001282678.2:c.1214G>A	NP_001269607.1:p.Cys405Tyr