Canonical Allele Identifier: CA843847297

Gene: PEX1

Linked Data

• dbSNP Id: rs1410485990
• gnomAD v3: 7-92502198-G-T
• gnomAD v4: 7-92502198-G-T
• MyVariant Identifiers: chr7:g.92131512G>T (hg19) ; chr7:g.92502198G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92502198G>T , CM000669.2:g.92502198G>T	GRCh38
NC_000007.13:g.92131512G>T , CM000669.1:g.92131512G>T	GRCh37
NC_000007.12:g.91969448G>T	NCBI36
NG_008341.1:g.31334C>A
NG_008341.2:g.31334C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.2227-119C>A MANE Select	ENSP00000248633.4:n.2227-119C>A
ENST00000248633.8:c.2227-119C>A	ENSP00000248633.4:n.2227-119C>A
ENST00000428214.5:c.2056-119C>A	ENSP00000394413.1:n.2056-119C>A
ENST00000438045.5:c.1261-119C>A	ENSP00000410438.1:n.1261-119C>A
ENST00000484913.5:n.2266-119C>A
ENST00000496092.1:n.25-119C>A
ENST00000496420.5:n.1903-119C>A
NM_000466.2:c.2227-119C>A	NP_000457.1:n.2227-119C>A
NM_001282677.1:c.2056-119C>A	NP_001269606.1:n.2056-119C>A
NM_001282678.1:c.1603-119C>A	NP_001269607.1:n.1603-119C>A
XM_005250433.3:c.478-119C>A	XP_005250490.1:n.478-119C>A
XR_242246.3:n.2323-119C>A
XM_017012319.2:c.478-119C>A	XP_016867808.1:n.478-119C>A
XR_001744808.2:n.1254-119C>A
XR_242246.5:n.2274-119C>A
NM_000466.3:c.2227-119C>A MANE Select	NP_000457.1:n.2227-119C>A
NM_001282677.2:c.2056-119C>A	NP_001269606.1:n.2056-119C>A
NM_001282678.2:c.1603-119C>A	NP_001269607.1:n.1603-119C>A