Canonical Allele Identifier: CA456481615

Gene: PEX1 GATAD1

Linked Data

• MyVariant Identifiers: chr7:g.92123862T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92494548T>G , CM000669.2:g.92494548T>G	GRCh38
NC_000007.13:g.92123862T>G , CM000669.1:g.92123862T>G	GRCh37
NC_000007.12:g.91961798T>G	NCBI36
NG_008341.1:g.38984A>C
NG_008341.2:g.38984A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.2865A>C (PEX1) MANE Select	ENSP00000248633.4:p.Gly955=
ENST00000248633.8:c.2865A>C (PEX1)	ENSP00000248633.4:p.Gly955=
ENST00000428214.5:c.2694A>C (PEX1)	ENSP00000394413.1:p.Gly898=
ENST00000438045.5:c.1899A>C (PEX1)	ENSP00000410438.1:p.Gly633=
ENST00000484913.5:n.2904A>C (PEX1)
ENST00000496420.5:n.2757A>C (PEX1)
NM_000466.2:c.2865A>C (PEX1)	NP_000457.1:p.Gly955=
NM_001282677.1:c.2694A>C (PEX1)	NP_001269606.1:p.Gly898=
NM_001282678.1:c.2241A>C (PEX1)	NP_001269607.1:p.Gly747=
XM_005250433.3:c.1116A>C (PEX1)	XP_005250490.1:p.Gly372=
XR_242246.3:n.2961A>C (PEX1)
XM_017012319.2:c.1116A>C (PEX1)	XP_016867808.1:p.Gly372=
XR_001744808.2:n.1892A>C (PEX1)
XR_001744843.2:n.5517T>G (GATAD1)
XR_242246.5:n.2912A>C (PEX1)
XR_927494.3:n.4368T>G (GATAD1)
XR_927503.3:n.4299T>G (GATAD1)
NM_000466.3:c.2865A>C (PEX1) MANE Select	NP_000457.1:p.Gly955=
NM_001282677.2:c.2694A>C (PEX1)	NP_001269606.1:p.Gly898=
NM_001282678.2:c.2241A>C (PEX1)	NP_001269607.1:p.Gly747=