Canonical Allele Identifier: CA368176826

Gene: PEX1

Linked Data

• MyVariant Identifiers: chr7:g.92131206T>C (hg19) ; chr7:g.92501892T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92501892T>C , CM000669.2:g.92501892T>C	GRCh38
NC_000007.13:g.92131206T>C , CM000669.1:g.92131206T>C	GRCh37
NC_000007.12:g.91969142T>C	NCBI36
NG_008341.1:g.31640A>G
NG_008341.2:g.31640A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000248633.9:c.2414A>G MANE Select	ENSP00000248633.4:p.Glu805Gly
ENST00000248633.8:c.2414A>G	ENSP00000248633.4:p.Glu805Gly
ENST00000428214.5:c.2243A>G	ENSP00000394413.1:p.Glu748Gly
ENST00000438045.5:c.1448A>G	ENSP00000410438.1:p.Glu483Gly
ENST00000484913.5:n.2453A>G
ENST00000496092.1:n.212A>G
ENST00000496420.5:n.2090A>G
NM_000466.2:c.2414A>G	NP_000457.1:p.Glu805Gly
NM_001282677.1:c.2243A>G	NP_001269606.1:p.Glu748Gly
NM_001282678.1:c.1790A>G	NP_001269607.1:p.Glu597Gly
XM_005250433.3:c.665A>G	XP_005250490.1:p.Glu222Gly
XR_242246.3:n.2510A>G
XM_017012319.2:c.665A>G	XP_016867808.1:p.Glu222Gly
XR_001744808.2:n.1441A>G
XR_242246.5:n.2461A>G
NM_000466.3:c.2414A>G MANE Select	NP_000457.1:p.Glu805Gly
NM_001282677.2:c.2243A>G	NP_001269606.1:p.Glu748Gly
NM_001282678.2:c.1790A>G	NP_001269607.1:p.Glu597Gly