Canonical Allele Identifier: CA576303776

Gene: PEX1

Linked Data

• dbSNP Id: rs1288735131
• gnomAD v2: 7-92126113-G-C
• gnomAD v4: 7-92496799-G-C
• MyVariant Identifiers: chr7:g.92126113G>C (hg19) ; chr7:g.92496799G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92496799G>C , CM000669.2:g.92496799G>C	GRCh38
NC_000007.13:g.92126113G>C , CM000669.1:g.92126113G>C	GRCh37
NC_000007.12:g.91964049G>C	NCBI36
NG_008341.1:g.36733C>G
NG_008341.2:g.36733C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000248633.9:c.2719-22C>G MANE Select	ENSP00000248633.4:n.2719-22C>G
ENST00000248633.8:c.2719-22C>G	ENSP00000248633.4:n.2719-22C>G
ENST00000428214.5:c.2548-22C>G	ENSP00000394413.1:n.2548-22C>G
ENST00000438045.5:c.1753-22C>G	ENSP00000410438.1:n.1753-22C>G
ENST00000484913.5:n.2758-22C>G
ENST00000496420.5:n.2611-22C>G
NM_000466.2:c.2719-22C>G	NP_000457.1:n.2719-22C>G
NM_001282677.1:c.2548-22C>G	NP_001269606.1:n.2548-22C>G
NM_001282678.1:c.2095-22C>G	NP_001269607.1:n.2095-22C>G
XM_005250433.3:c.970-22C>G	XP_005250490.1:n.970-22C>G
XR_242246.3:n.2815-22C>G
XM_017012319.2:c.970-22C>G	XP_016867808.1:n.970-22C>G
XR_001744808.2:n.1746-22C>G
XR_242246.5:n.2766-22C>G
NM_000466.3:c.2719-22C>G MANE Select	NP_000457.1:n.2719-22C>G
NM_001282677.2:c.2548-22C>G	NP_001269606.1:n.2548-22C>G
NM_001282678.2:c.2095-22C>G	NP_001269607.1:n.2095-22C>G