Canonical Allele Identifier: CA368173780

Gene: PEX1

Linked Data

• MyVariant Identifiers: chr7:g.92129080C>G (hg19) ; chr7:g.92499766C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92499766C>G , CM000669.2:g.92499766C>G	GRCh38
NC_000007.13:g.92129080C>G , CM000669.1:g.92129080C>G	GRCh37
NC_000007.12:g.91967016C>G	NCBI36
NG_008341.1:g.33766G>C
NG_008341.2:g.33766G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.2656G>C MANE Select	ENSP00000248633.4:p.Gly886Arg
ENST00000248633.8:c.2656G>C	ENSP00000248633.4:p.Gly886Arg
ENST00000428214.5:c.2485G>C	ENSP00000394413.1:p.Gly829Arg
ENST00000438045.5:c.1690G>C	ENSP00000410438.1:p.Gly564Arg
ENST00000484913.5:n.2695G>C
ENST00000496420.5:n.2548G>C
NM_000466.2:c.2656G>C	NP_000457.1:p.Gly886Arg
NM_001282677.1:c.2485G>C	NP_001269606.1:p.Gly829Arg
NM_001282678.1:c.2032G>C	NP_001269607.1:p.Gly678Arg
XM_005250433.3:c.907G>C	XP_005250490.1:p.Gly303Arg
XR_242246.3:n.2752G>C
XM_017012319.2:c.907G>C	XP_016867808.1:p.Gly303Arg
XR_001744808.2:n.1683G>C
XR_242246.5:n.2703G>C
NM_000466.3:c.2656G>C MANE Select	NP_000457.1:p.Gly886Arg
NM_001282677.2:c.2485G>C	NP_001269606.1:p.Gly829Arg
NM_001282678.2:c.2032G>C	NP_001269607.1:p.Gly678Arg