Canonical Allele Identifier: CA368184640

Gene: PEX1

Linked Data

• MyVariant Identifiers: chr7:g.92135577A>C (hg19) ; chr7:g.92506263A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92506263A>C , CM000669.2:g.92506263A>C	GRCh38
NC_000007.13:g.92135577A>C , CM000669.1:g.92135577A>C	GRCh37
NC_000007.12:g.91973513A>C	NCBI36
NG_008341.1:g.27269T>G
NG_008341.2:g.27269T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.1885T>G MANE Select	ENSP00000248633.4:p.Cys629Gly
ENST00000248633.8:c.1885T>G	ENSP00000248633.4:p.Cys629Gly
ENST00000422866.1:c.703T>G
ENST00000428214.5:c.1885T>G	ENSP00000394413.1:p.Cys629Gly
ENST00000438045.5:c.919T>G	ENSP00000410438.1:p.Cys307Gly
ENST00000484913.5:n.1924T>G
ENST00000496420.5:n.1561T>G
NM_000466.2:c.1885T>G	NP_000457.1:p.Cys629Gly
NM_001282677.1:c.1885T>G	NP_001269606.1:p.Cys629Gly
NM_001282678.1:c.1261T>G	NP_001269607.1:p.Cys421Gly
XM_005250433.3:c.136T>G	XP_005250490.1:p.Cys46Gly
XR_242246.3:n.1981T>G
XM_017012319.2:c.136T>G	XP_016867808.1:p.Cys46Gly
XR_001744808.2:n.912T>G
XR_242246.5:n.1932T>G
NM_000466.3:c.1885T>G MANE Select	NP_000457.1:p.Cys629Gly
NM_001282677.2:c.1885T>G	NP_001269606.1:p.Cys629Gly
NM_001282678.2:c.1261T>G	NP_001269607.1:p.Cys421Gly