Canonical Allele Identifier: CA368183988

Gene: PEX1

Linked Data - Variant Effect Evidence

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92504864C>G , CM000669.2:g.92504864C>G	GRCh38
NC_000007.13:g.92134178C>G , CM000669.1:g.92134178C>G	GRCh37
NC_000007.12:g.91972114C>G	NCBI36
NG_008341.1:g.28668G>C
NG_008341.2:g.28668G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.1939G>C MANE Select	ENSP00000248633.4:p.Ala647Pro
ENST00000248633.8:c.1939G>C	ENSP00000248633.4:p.Ala647Pro
ENST00000428214.5:c.1900+1384G>C	ENSP00000394413.1:n.1900+1384G>C
ENST00000438045.5:c.973G>C	ENSP00000410438.1:p.Ala325Pro
ENST00000484913.5:n.1978G>C
ENST00000496420.5:n.1615G>C
NM_000466.2:c.1939G>C	NP_000457.1:p.Ala647Pro
NM_001282677.1:c.1900+1384G>C	NP_001269606.1:n.1900+1384G>C
NM_001282678.1:c.1315G>C	NP_001269607.1:p.Ala439Pro
XM_005250433.3:c.190G>C	XP_005250490.1:p.Ala64Pro
XR_242246.3:n.2035G>C
XM_017012319.2:c.190G>C	XP_016867808.1:p.Ala64Pro
XR_001744808.2:n.966G>C
XR_242246.5:n.1986G>C
NM_000466.3:c.1939G>C MANE Select	NP_000457.1:p.Ala647Pro
NM_001282677.2:c.1900+1384G>C	NP_001269606.1:n.1900+1384G>C
NM_001282678.2:c.1315G>C	NP_001269607.1:p.Ala439Pro