Canonical Allele Identifier: CA843856466

Gene: PEX1

Linked Data

• dbSNP Id: rs1412210846
• gnomAD v4: 7-92517180-G-T
• MyVariant Identifiers: chr7:g.92146494G>T (hg19) ; chr7:g.92517180G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92517180G>T , CM000669.2:g.92517180G>T	GRCh38
NC_000007.13:g.92146494G>T , CM000669.1:g.92146494G>T	GRCh37
NC_000007.12:g.91984430G>T	NCBI36
NG_008341.1:g.16352C>A
NG_008341.2:g.16352C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.1239+96C>A MANE Select	ENSP00000248633.4:n.1239+96C>A
ENST00000248633.8:c.1239+96C>A	ENSP00000248633.4:n.1239+96C>A
ENST00000422866.1:c.140+96C>A
ENST00000428214.5:c.1239+96C>A	ENSP00000394413.1:n.1239+96C>A
ENST00000438045.5:c.274-3213C>A	ENSP00000410438.1:n.274-3213C>A
ENST00000484913.5:n.1278+96C>A
NM_000466.2:c.1239+96C>A	NP_000457.1:n.1239+96C>A
NM_001282677.1:c.1239+96C>A	NP_001269606.1:n.1239+96C>A
NM_001282678.1:c.615+96C>A	NP_001269607.1:n.615+96C>A
XR_242246.3:n.1335+96C>A
XM_017012319.2:c.-428+96C>A	XP_016867808.1:n.-428+96C>A
XR_001744808.2:n.349+96C>A
XR_242246.5:n.1286+96C>A
NM_000466.3:c.1239+96C>A MANE Select	NP_000457.1:n.1239+96C>A
NM_001282677.2:c.1239+96C>A	NP_001269606.1:n.1239+96C>A
NM_001282678.2:c.615+96C>A	NP_001269607.1:n.615+96C>A