Canonical Allele Identifier: CA368167282

Gene: PEX1 GATAD1

Linked Data

• MyVariant Identifiers: chr7:g.92123612C>G (hg19) ; chr7:g.92494298C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92494298C>G , CM000669.2:g.92494298C>G	GRCh38
NC_000007.13:g.92123612C>G , CM000669.1:g.92123612C>G	GRCh37
NC_000007.12:g.91961548C>G	NCBI36
NG_008341.1:g.39234G>C
NG_008341.2:g.39234G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000248633.9:c.3025G>C (PEX1) MANE Select	ENSP00000248633.4:p.Asp1009His
ENST00000248633.8:c.3025G>C (PEX1)	ENSP00000248633.4:p.Asp1009His
ENST00000428214.5:c.2854G>C (PEX1)	ENSP00000394413.1:p.Asp952His
ENST00000438045.5:c.2059G>C (PEX1)	ENSP00000410438.1:p.Asp687His
ENST00000484913.5:n.3064G>C (PEX1)
ENST00000496420.5:n.2917G>C (PEX1)
NM_000466.2:c.3025G>C (PEX1)	NP_000457.1:p.Asp1009His
NM_001282677.1:c.2854G>C (PEX1)	NP_001269606.1:p.Asp952His
NM_001282678.1:c.2401G>C (PEX1)	NP_001269607.1:p.Asp801His
XM_005250433.3:c.1276G>C (PEX1)	XP_005250490.1:p.Asp426His
XR_242246.3:n.3121G>C (PEX1)
XM_017012319.2:c.1276G>C (PEX1)	XP_016867808.1:p.Asp426His
XR_001744808.2:n.2052G>C (PEX1)
XR_001744843.2:n.5267C>G (GATAD1)
XR_242246.5:n.3072G>C (PEX1)
XR_927494.3:n.4118C>G (GATAD1)
XR_927503.3:n.4049C>G (GATAD1)
NM_000466.3:c.3025G>C (PEX1) MANE Select	NP_000457.1:p.Asp1009His
NM_001282677.2:c.2854G>C (PEX1)	NP_001269606.1:p.Asp952His
NM_001282678.2:c.2401G>C (PEX1)	NP_001269607.1:p.Asp801His