Canonical Allele Identifier: CA368160776

Gene: PEX1 GATAD1

Linked Data

• MyVariant Identifiers: chr7:g.92119038C>G (hg19) ; chr7:g.92489724C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92489724C>G , CM000669.2:g.92489724C>G	GRCh38
NC_000007.13:g.92119038C>G , CM000669.1:g.92119038C>G	GRCh37
NC_000007.12:g.91956974C>G	NCBI36
NG_008341.1:g.43808G>C
NG_008341.2:g.43808G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000248633.9:c.3626G>C (PEX1) MANE Select	ENSP00000248633.4:p.Ser1209Thr
ENST00000248633.8:c.3626G>C (PEX1)	ENSP00000248633.4:p.Ser1209Thr
ENST00000428214.5:c.3455G>C (PEX1)	ENSP00000394413.1:p.Ser1152Thr
ENST00000438045.5:c.2660G>C (PEX1)	ENSP00000410438.1:p.Ser887Thr
ENST00000469417.1:n.523G>C (PEX1)
ENST00000477342.1:n.71G>C (PEX1)
ENST00000484913.5:n.3665G>C (PEX1)
ENST00000496420.5:n.4681G>C (PEX1)
NM_000466.2:c.3626G>C (PEX1)	NP_000457.1:p.Ser1209Thr
NM_001282677.1:c.3455G>C (PEX1)	NP_001269606.1:p.Ser1152Thr
NM_001282678.1:c.3002G>C (PEX1)	NP_001269607.1:p.Ser1001Thr
XM_005250433.3:c.1877G>C (PEX1)	XP_005250490.1:p.Ser626Thr
XR_242246.3:n.3722G>C (PEX1)
XR_927494.1:n.1036-1519C>G (GATAD1)
XR_927495.1:n.1036-362C>G (GATAD1)
XR_927496.1:n.1041-1519C>G (GATAD1)
XR_927497.1:n.1036-362C>G (GATAD1)
XR_927498.1:n.1124-1519C>G (GATAD1)
XR_927500.1:n.1033-1519C>G (GATAD1)
XR_927502.1:n.1033-362C>G (GATAD1)
XR_927503.1:n.967-1519C>G (GATAD1)
XM_017012319.2:c.1877G>C (PEX1)	XP_016867808.1:p.Ser626Thr
XR_001744808.2:n.2653G>C (PEX1)
XR_001744842.2:n.2281-1519C>G (GATAD1)
XR_001744843.2:n.2212-1519C>G (GATAD1)
XR_002956472.1:n.2281-362C>G (GATAD1)
XR_002956473.1:n.2369-1519C>G (GATAD1)
XR_002956474.1:n.2286-1519C>G (GATAD1)
XR_242246.5:n.3673G>C (PEX1)
XR_927494.3:n.1063-1519C>G (GATAD1)
XR_927500.3:n.1060-1519C>G (GATAD1)
XR_927503.3:n.994-1519C>G (GATAD1)
NM_000466.3:c.3626G>C (PEX1) MANE Select	NP_000457.1:p.Ser1209Thr
NM_001282677.2:c.3455G>C (PEX1)	NP_001269606.1:p.Ser1152Thr
NM_001282678.2:c.3002G>C (PEX1)	NP_001269607.1:p.Ser1001Thr