Canonical Allele Identifier: CA368184563

Gene: PEX1

Linked Data

• gnomAD v4: 7-92506253-A-G
• MyVariant Identifiers: chr7:g.92135567A>G (hg19) ; chr7:g.92506253A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92506253A>G , CM000669.2:g.92506253A>G	GRCh38
NC_000007.13:g.92135567A>G , CM000669.1:g.92135567A>G	GRCh37
NC_000007.12:g.91973503A>G	NCBI36
NG_008341.1:g.27279T>C
NG_008341.2:g.27279T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000248633.9:c.1895T>C MANE Select	ENSP00000248633.4:p.Leu632Ser
ENST00000248633.8:c.1895T>C	ENSP00000248633.4:p.Leu632Ser
ENST00000422866.1:c.713T>C
ENST00000428214.5:c.1895T>C	ENSP00000394413.1:p.Leu632Ser
ENST00000438045.5:c.929T>C	ENSP00000410438.1:p.Leu310Ser
ENST00000484913.5:n.1934T>C
ENST00000496420.5:n.1571T>C
NM_000466.2:c.1895T>C	NP_000457.1:p.Leu632Ser
NM_001282677.1:c.1895T>C	NP_001269606.1:p.Leu632Ser
NM_001282678.1:c.1271T>C	NP_001269607.1:p.Leu424Ser
XM_005250433.3:c.146T>C	XP_005250490.1:p.Leu49Ser
XR_242246.3:n.1991T>C
XM_017012319.2:c.146T>C	XP_016867808.1:p.Leu49Ser
XR_001744808.2:n.922T>C
XR_242246.5:n.1942T>C
NM_000466.3:c.1895T>C MANE Select	NP_000457.1:p.Leu632Ser
NM_001282677.2:c.1895T>C	NP_001269606.1:p.Leu632Ser
NM_001282678.2:c.1271T>C	NP_001269607.1:p.Leu424Ser