Canonical Allele Identifier: CA368202968

Gene: PEX1

Linked Data - Variant Effect Evidence

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92519015C>G , CM000669.2:g.92519015C>G	GRCh38
NC_000007.13:g.92148329C>G , CM000669.1:g.92148329C>G	GRCh37
NC_000007.12:g.91986265C>G	NCBI36
NG_008341.1:g.14517G>C
NG_008341.2:g.14517G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.337G>C MANE Select	ENSP00000248633.4:p.Ala113Pro
ENST00000248633.8:c.337G>C	ENSP00000248633.4:p.Ala113Pro
ENST00000428214.5:c.337G>C	ENSP00000394413.1:p.Ala113Pro
ENST00000438045.5:c.273+3087G>C	ENSP00000410438.1:n.273+3087G>C
ENST00000484913.5:n.341G>C
NM_000466.2:c.337G>C	NP_000457.1:p.Ala113Pro
NM_001282677.1:c.337G>C	NP_001269606.1:p.Ala113Pro
NM_001282678.1:c.-323G>C	NP_001269607.1:n.-323G>C
XR_242246.3:n.433G>C
XR_242246.5:n.384G>C
NM_000466.3:c.337G>C MANE Select	NP_000457.1:p.Ala113Pro
NM_001282677.2:c.337G>C	NP_001269606.1:p.Ala113Pro
NM_001282678.2:c.-323G>C	NP_001269607.1:n.-323G>C