Canonical Allele Identifier: CA368190352

Gene: PEX1

Linked Data

• MyVariant Identifiers: chr7:g.92140346G>C (hg19) ; chr7:g.92511032G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92511032G>C , CM000669.2:g.92511032G>C	GRCh38
NC_000007.13:g.92140346G>C , CM000669.1:g.92140346G>C	GRCh37
NC_000007.12:g.91978282G>C	NCBI36
NG_008341.1:g.22500C>G
NG_008341.2:g.22500C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.1499C>G MANE Select	ENSP00000248633.4:p.Ser500Cys
ENST00000248633.8:c.1499C>G	ENSP00000248633.4:p.Ser500Cys
ENST00000422866.1:c.400C>G
ENST00000428214.5:c.1499C>G	ENSP00000394413.1:p.Ser500Cys
ENST00000438045.5:c.533C>G	ENSP00000410438.1:p.Ser178Cys
ENST00000476923.1:n.260C>G
ENST00000484913.5:n.1538C>G
NM_000466.2:c.1499C>G	NP_000457.1:p.Ser500Cys
NM_001282677.1:c.1499C>G	NP_001269606.1:p.Ser500Cys
NM_001282678.1:c.875C>G	NP_001269607.1:p.Ser292Cys
XM_005250433.3:c.-168C>G	XP_005250490.1:n.-168C>G
XR_242246.3:n.1595C>G
XM_017012319.2:c.-168C>G	XP_016867808.1:n.-168C>G
XR_001744808.2:n.609C>G
XR_242246.5:n.1546C>G
NM_000466.3:c.1499C>G MANE Select	NP_000457.1:p.Ser500Cys
NM_001282677.2:c.1499C>G	NP_001269606.1:p.Ser500Cys
NM_001282678.2:c.875C>G	NP_001269607.1:p.Ser292Cys