Canonical Allele Identifier: CA456482928

Gene: PEX1

Linked Data

• MyVariant Identifiers: chr7:g.92131277A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92501963A>C , CM000669.2:g.92501963A>C	GRCh38
NC_000007.13:g.92131277A>C , CM000669.1:g.92131277A>C	GRCh37
NC_000007.12:g.91969213A>C	NCBI36
NG_008341.1:g.31569T>G
NG_008341.2:g.31569T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.2343T>G MANE Select	ENSP00000248633.4:p.Ala781=
ENST00000248633.8:c.2343T>G	ENSP00000248633.4:p.Ala781=
ENST00000428214.5:c.2172T>G	ENSP00000394413.1:p.Ala724=
ENST00000438045.5:c.1377T>G	ENSP00000410438.1:p.Ala459=
ENST00000484913.5:n.2382T>G
ENST00000496092.1:n.141T>G
ENST00000496420.5:n.2019T>G
NM_000466.2:c.2343T>G	NP_000457.1:p.Ala781=
NM_001282677.1:c.2172T>G	NP_001269606.1:p.Ala724=
NM_001282678.1:c.1719T>G	NP_001269607.1:p.Ala573=
XM_005250433.3:c.594T>G	XP_005250490.1:p.Ala198=
XR_242246.3:n.2439T>G
XM_017012319.2:c.594T>G	XP_016867808.1:p.Ala198=
XR_001744808.2:n.1370T>G
XR_242246.5:n.2390T>G
NM_000466.3:c.2343T>G MANE Select	NP_000457.1:p.Ala781=
NM_001282677.2:c.2172T>G	NP_001269606.1:p.Ala724=
NM_001282678.2:c.1719T>G	NP_001269607.1:p.Ala573=