Canonical Allele Identifier: CA368181812

Gene: PEX1

Linked Data

• MyVariant Identifiers: chr7:g.92132450T>A (hg19) ; chr7:g.92503136T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92503136T>A , CM000669.2:g.92503136T>A	GRCh38
NC_000007.13:g.92132450T>A , CM000669.1:g.92132450T>A	GRCh37
NC_000007.12:g.91970386T>A	NCBI36
NG_008341.1:g.30396A>T
NG_008341.2:g.30396A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.2131A>T MANE Select	ENSP00000248633.4:p.Thr711Ser
ENST00000248633.8:c.2131A>T	ENSP00000248633.4:p.Thr711Ser
ENST00000428214.5:c.1960A>T	ENSP00000394413.1:p.Thr654Ser
ENST00000438045.5:c.1165A>T	ENSP00000410438.1:p.Thr389Ser
ENST00000484913.5:n.2170A>T
ENST00000496420.5:n.1807A>T
NM_000466.2:c.2131A>T	NP_000457.1:p.Thr711Ser
NM_001282677.1:c.1960A>T	NP_001269606.1:p.Thr654Ser
NM_001282678.1:c.1507A>T	NP_001269607.1:p.Thr503Ser
XM_005250433.3:c.382A>T	XP_005250490.1:p.Thr128Ser
XR_242246.3:n.2227A>T
XM_017012319.2:c.382A>T	XP_016867808.1:p.Thr128Ser
XR_001744808.2:n.1158A>T
XR_242246.5:n.2178A>T
NM_000466.3:c.2131A>T MANE Select	NP_000457.1:p.Thr711Ser
NM_001282677.2:c.1960A>T	NP_001269606.1:p.Thr654Ser
NM_001282678.2:c.1507A>T	NP_001269607.1:p.Thr503Ser