Canonical Allele Identifier: CA4341473

Gene: PEX1

Linked Data

• dbSNP Id: rs772086409
• ExAC: 7:92146630 T / C
• gnomAD v2: 7-92146630-T-C
• MyVariant Identifiers: chr7:g.92146630T>C (hg19) ; chr7:g.92517316T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92517316T>C , CM000669.2:g.92517316T>C	GRCh38
NC_000007.13:g.92146630T>C , CM000669.1:g.92146630T>C	GRCh37
NC_000007.12:g.91984566T>C	NCBI36
NG_008341.1:g.16216A>G
NG_008341.2:g.16216A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.1199A>G MANE Select	ENSP00000248633.4:p.Tyr400Cys
ENST00000248633.8:c.1199A>G	ENSP00000248633.4:p.Tyr400Cys
ENST00000422866.1:c.100A>G
ENST00000428214.5:c.1199A>G	ENSP00000394413.1:p.Tyr400Cys
ENST00000438045.5:c.274-3349A>G	ENSP00000410438.1:n.274-3349A>G
ENST00000484913.5:n.1238A>G
NM_000466.2:c.1199A>G	NP_000457.1:p.Tyr400Cys
NM_001282677.1:c.1199A>G	NP_001269606.1:p.Tyr400Cys
NM_001282678.1:c.575A>G	NP_001269607.1:p.Tyr192Cys
XR_242246.3:n.1295A>G
XM_017012319.2:c.-468A>G	XP_016867808.1:n.-468A>G
XR_001744808.2:n.309A>G
XR_242246.5:n.1246A>G
NM_000466.3:c.1199A>G MANE Select	NP_000457.1:p.Tyr400Cys
NM_001282677.2:c.1199A>G	NP_001269606.1:p.Tyr400Cys
NM_001282678.2:c.575A>G	NP_001269607.1:p.Tyr192Cys