Canonical Allele Identifier: CA843850163

Gene: PEX1

Linked Data

• dbSNP Id: rs1421662635
• gnomAD v3: 7-92506386-T-C
• gnomAD v4: 7-92506386-T-C
• MyVariant Identifiers: chr7:g.92135700T>C (hg19) ; chr7:g.92506386T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92506386T>C , CM000669.2:g.92506386T>C	GRCh38
NC_000007.13:g.92135700T>C , CM000669.1:g.92135700T>C	GRCh37
NC_000007.12:g.91973636T>C	NCBI36
NG_008341.1:g.27146A>G
NG_008341.2:g.27146A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.1804-42A>G MANE Select	ENSP00000248633.4:n.1804-42A>G
ENST00000248633.8:c.1804-42A>G	ENSP00000248633.4:n.1804-42A>G
ENST00000422866.1:c.622-42A>G
ENST00000428214.5:c.1804-42A>G	ENSP00000394413.1:n.1804-42A>G
ENST00000438045.5:c.838-42A>G	ENSP00000410438.1:n.838-42A>G
ENST00000484913.5:n.1843-42A>G
ENST00000496420.5:n.1438A>G
NM_000466.2:c.1804-42A>G	NP_000457.1:n.1804-42A>G
NM_001282677.1:c.1804-42A>G	NP_001269606.1:n.1804-42A>G
NM_001282678.1:c.1180-42A>G	NP_001269607.1:n.1180-42A>G
XM_005250433.3:c.55-42A>G	XP_005250490.1:n.55-42A>G
XR_242246.3:n.1900-42A>G
XM_017012319.2:c.55-42A>G	XP_016867808.1:n.55-42A>G
XR_001744808.2:n.831-42A>G
XR_242246.5:n.1851-42A>G
NM_000466.3:c.1804-42A>G MANE Select	NP_000457.1:n.1804-42A>G
NM_001282677.2:c.1804-42A>G	NP_001269606.1:n.1804-42A>G
NM_001282678.2:c.1180-42A>G	NP_001269607.1:n.1180-42A>G