Canonical Allele Identifier: CA2683721244

Gene: PEX1

Linked Data

• gnomAD v4: 7-92522011-TCC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92522012_92522013del , CM000669.2:g.92522012_92522013del	GRCh38
NC_000007.13:g.92151326_92151327del , CM000669.1:g.92151326_92151327del	GRCh37
NC_000007.12:g.91989262_91989263del	NCBI36
NG_008341.1:g.11519_11520del
NG_008341.2:g.11519_11520del

Transcript Alleles

HGVS	Amino-acid change
ENST00000248633.9:c.273+89_273+90del MANE Select	ENSP00000248633.4:n.273+89_273+90del
ENST00000248633.8:c.273+89_273+90del	ENSP00000248633.4:n.273+89_273+90del
ENST00000428214.5:c.273+89_273+90del	ENSP00000394413.1:n.273+89_273+90del
ENST00000438045.5:c.273+89_273+90del	ENSP00000410438.1:n.273+89_273+90del
ENST00000484913.5:n.277+89_277+90del
NM_000466.2:c.273+89_273+90del	NP_000457.1:n.273+89_273+90del
NM_001282677.1:c.273+89_273+90del	NP_001269606.1:n.273+89_273+90del
NM_001282678.1:c.-387+89_-387+90del	NP_001269607.1:n.-387+89_-387+90del
XR_242246.3:n.369+89_369+90del
XR_242246.5:n.320+89_320+90del
NM_000466.3:c.273+89_273+90del MANE Select	NP_000457.1:n.273+89_273+90del
NM_001282677.2:c.273+89_273+90del	NP_001269606.1:n.273+89_273+90del
NM_001282678.2:c.-387+89_-387+90del	NP_001269607.1:n.-387+89_-387+90del