Canonical Allele Identifier: CA2683720293

Gene: PEX1

Linked Data

• gnomAD v4: 7-92509237-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92509237A>G , CM000669.2:g.92509237A>G	GRCh38
NC_000007.13:g.92138551A>G , CM000669.1:g.92138551A>G	GRCh37
NC_000007.12:g.91976487A>G	NCBI36
NG_008341.1:g.24295T>C
NG_008341.2:g.24295T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.1670+92T>C MANE Select	ENSP00000248633.4:n.1670+92T>C
ENST00000248633.8:c.1670+92T>C	ENSP00000248633.4:n.1670+92T>C
ENST00000422866.1:c.488+1707T>C
ENST00000428214.5:c.1670+92T>C	ENSP00000394413.1:n.1670+92T>C
ENST00000438045.5:c.704+92T>C	ENSP00000410438.1:n.704+92T>C
ENST00000484913.5:n.1709+92T>C
NM_000466.2:c.1670+92T>C	NP_000457.1:n.1670+92T>C
NM_001282677.1:c.1670+92T>C	NP_001269606.1:n.1670+92T>C
NM_001282678.1:c.1046+92T>C	NP_001269607.1:n.1046+92T>C
XM_005250433.3:c.-80+1707T>C	XP_005250490.1:n.-80+1707T>C
XR_242246.3:n.1766+92T>C
XM_017012319.2:c.-80+1707T>C	XP_016867808.1:n.-80+1707T>C
XR_001744808.2:n.697+1707T>C
XR_242246.5:n.1717+92T>C
NM_000466.3:c.1670+92T>C MANE Select	NP_000457.1:n.1670+92T>C
NM_001282677.2:c.1670+92T>C	NP_001269606.1:n.1670+92T>C
NM_001282678.2:c.1046+92T>C	NP_001269607.1:n.1046+92T>C