Canonical Allele Identifier: CA368170883

Gene: PEX1

Linked Data

• MyVariant Identifiers: chr7:g.92126036A>T (hg19) ; chr7:g.92496722A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92496722A>T , CM000669.2:g.92496722A>T	GRCh38
NC_000007.13:g.92126036A>T , CM000669.1:g.92126036A>T	GRCh37
NC_000007.12:g.91963972A>T	NCBI36
NG_008341.1:g.36810T>A
NG_008341.2:g.36810T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000248633.9:c.2774T>A MANE Select	ENSP00000248633.4:p.Ile925Asn
ENST00000248633.8:c.2774T>A	ENSP00000248633.4:p.Ile925Asn
ENST00000428214.5:c.2603T>A	ENSP00000394413.1:p.Ile868Asn
ENST00000438045.5:c.1808T>A	ENSP00000410438.1:p.Ile603Asn
ENST00000484913.5:n.2813T>A
ENST00000496420.5:n.2666T>A
NM_000466.2:c.2774T>A	NP_000457.1:p.Ile925Asn
NM_001282677.1:c.2603T>A	NP_001269606.1:p.Ile868Asn
NM_001282678.1:c.2150T>A	NP_001269607.1:p.Ile717Asn
XM_005250433.3:c.1025T>A	XP_005250490.1:p.Ile342Asn
XR_242246.3:n.2870T>A
XM_017012319.2:c.1025T>A	XP_016867808.1:p.Ile342Asn
XR_001744808.2:n.1801T>A
XR_242246.5:n.2821T>A
NM_000466.3:c.2774T>A MANE Select	NP_000457.1:p.Ile925Asn
NM_001282677.2:c.2603T>A	NP_001269606.1:p.Ile868Asn
NM_001282678.2:c.2150T>A	NP_001269607.1:p.Ile717Asn