Canonical Allele Identifier: CA456483239

Gene: PEX1

Linked Data

• MyVariant Identifiers: chr7:g.92132502A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92503188A>G , CM000669.2:g.92503188A>G	GRCh38
NC_000007.13:g.92132502A>G , CM000669.1:g.92132502A>G	GRCh37
NC_000007.12:g.91970438A>G	NCBI36
NG_008341.1:g.30344T>C
NG_008341.2:g.30344T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000248633.9:c.2079T>C MANE Select	ENSP00000248633.4:p.Asn693=
ENST00000248633.8:c.2079T>C	ENSP00000248633.4:p.Asn693=
ENST00000428214.5:c.1908T>C	ENSP00000394413.1:p.Asn636=
ENST00000438045.5:c.1113T>C	ENSP00000410438.1:p.Asn371=
ENST00000484913.5:n.2118T>C
ENST00000496420.5:n.1755T>C
NM_000466.2:c.2079T>C	NP_000457.1:p.Asn693=
NM_001282677.1:c.1908T>C	NP_001269606.1:p.Asn636=
NM_001282678.1:c.1455T>C	NP_001269607.1:p.Asn485=
XM_005250433.3:c.330T>C	XP_005250490.1:p.Asn110=
XR_242246.3:n.2175T>C
XM_017012319.2:c.330T>C	XP_016867808.1:p.Asn110=
XR_001744808.2:n.1106T>C
XR_242246.5:n.2126T>C
NM_000466.3:c.2079T>C MANE Select	NP_000457.1:p.Asn693=
NM_001282677.2:c.1908T>C	NP_001269606.1:p.Asn636=
NM_001282678.2:c.1455T>C	NP_001269607.1:p.Asn485=