Canonical Allele Identifier: CA368183714

Gene: PEX1

Linked Data

• MyVariant Identifiers: chr7:g.92134154G>C (hg19) ; chr7:g.92504840G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92504840G>C , CM000669.2:g.92504840G>C	GRCh38
NC_000007.13:g.92134154G>C , CM000669.1:g.92134154G>C	GRCh37
NC_000007.12:g.91972090G>C	NCBI36
NG_008341.1:g.28692C>G
NG_008341.2:g.28692C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.1963C>G MANE Select	ENSP00000248633.4:p.Gln655Glu
ENST00000248633.8:c.1963C>G	ENSP00000248633.4:p.Gln655Glu
ENST00000428214.5:c.1900+1408C>G	ENSP00000394413.1:n.1900+1408C>G
ENST00000438045.5:c.997C>G	ENSP00000410438.1:p.Gln333Glu
ENST00000484913.5:n.2002C>G
ENST00000496420.5:n.1639C>G
NM_000466.2:c.1963C>G	NP_000457.1:p.Gln655Glu
NM_001282677.1:c.1900+1408C>G	NP_001269606.1:n.1900+1408C>G
NM_001282678.1:c.1339C>G	NP_001269607.1:p.Gln447Glu
XM_005250433.3:c.214C>G	XP_005250490.1:p.Gln72Glu
XR_242246.3:n.2059C>G
XM_017012319.2:c.214C>G	XP_016867808.1:p.Gln72Glu
XR_001744808.2:n.990C>G
XR_242246.5:n.2010C>G
NM_000466.3:c.1963C>G MANE Select	NP_000457.1:p.Gln655Glu
NM_001282677.2:c.1900+1408C>G	NP_001269606.1:n.1900+1408C>G
NM_001282678.2:c.1339C>G	NP_001269607.1:p.Gln447Glu