Canonical Allele Identifier: CA456481976

Gene: PEX1

Linked Data

• gnomAD v4: 7-92499754-G-A
• MyVariant Identifiers: chr7:g.92129068G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92499754G>A , CM000669.2:g.92499754G>A	GRCh38
NC_000007.13:g.92129068G>A , CM000669.1:g.92129068G>A	GRCh37
NC_000007.12:g.91967004G>A	NCBI36
NG_008341.1:g.33778C>T
NG_008341.2:g.33778C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.2668C>T MANE Select	ENSP00000248633.4:p.Leu890=
ENST00000248633.8:c.2668C>T	ENSP00000248633.4:p.Leu890=
ENST00000428214.5:c.2497C>T	ENSP00000394413.1:p.Leu833=
ENST00000438045.5:c.1702C>T	ENSP00000410438.1:p.Leu568=
ENST00000484913.5:n.2707C>T
ENST00000496420.5:n.2560C>T
NM_000466.2:c.2668C>T	NP_000457.1:p.Leu890=
NM_001282677.1:c.2497C>T	NP_001269606.1:p.Leu833=
NM_001282678.1:c.2044C>T	NP_001269607.1:p.Leu682=
XM_005250433.3:c.919C>T	XP_005250490.1:p.Leu307=
XR_242246.3:n.2764C>T
XM_017012319.2:c.919C>T	XP_016867808.1:p.Leu307=
XR_001744808.2:n.1695C>T
XR_242246.5:n.2715C>T
NM_000466.3:c.2668C>T MANE Select	NP_000457.1:p.Leu890=
NM_001282677.2:c.2497C>T	NP_001269606.1:p.Leu833=
NM_001282678.2:c.2044C>T	NP_001269607.1:p.Leu682=