Canonical Allele Identifier: CA368188737

Gene: PEX1

Linked Data

• MyVariant Identifiers: chr7:g.92140269T>G (hg19) ; chr7:g.92510955T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92510955T>G , CM000669.2:g.92510955T>G	GRCh38
NC_000007.13:g.92140269T>G , CM000669.1:g.92140269T>G	GRCh37
NC_000007.12:g.91978205T>G	NCBI36
NG_008341.1:g.22577A>C
NG_008341.2:g.22577A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000248633.9:c.1576A>C MANE Select	ENSP00000248633.4:p.Thr526Pro
ENST00000248633.8:c.1576A>C	ENSP00000248633.4:p.Thr526Pro
ENST00000422866.1:c.477A>C
ENST00000428214.5:c.1576A>C	ENSP00000394413.1:p.Thr526Pro
ENST00000438045.5:c.610A>C	ENSP00000410438.1:p.Thr204Pro
ENST00000476923.1:n.337A>C
ENST00000484913.5:n.1615A>C
NM_000466.2:c.1576A>C	NP_000457.1:p.Thr526Pro
NM_001282677.1:c.1576A>C	NP_001269606.1:p.Thr526Pro
NM_001282678.1:c.952A>C	NP_001269607.1:p.Thr318Pro
XM_005250433.3:c.-91A>C	XP_005250490.1:n.-91A>C
XR_242246.3:n.1672A>C
XM_017012319.2:c.-91A>C	XP_016867808.1:n.-91A>C
XR_001744808.2:n.686A>C
XR_242246.5:n.1623A>C
NM_000466.3:c.1576A>C MANE Select	NP_000457.1:p.Thr526Pro
NM_001282677.2:c.1576A>C	NP_001269606.1:p.Thr526Pro
NM_001282678.2:c.952A>C	NP_001269607.1:p.Thr318Pro