Canonical Allele Identifier: CA2776947688

Gene: PEX1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92522334_92522335insACA , CM000669.2:g.92522334_92522335insACA	GRCh38
NC_000007.13:g.92151648_92151649insACA , CM000669.1:g.92151648_92151649insACA	GRCh37
NC_000007.12:g.91989584_91989585insACA	NCBI36
NG_008341.1:g.11197_11198insTGT
NG_008341.2:g.11197_11198insTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.130-90_130-89insTGT MANE Select	ENSP00000248633.4:n.130-90_130-89insTGT
ENST00000248633.8:c.130-90_130-89insTGT	ENSP00000248633.4:n.130-90_130-89insTGT
ENST00000428214.5:c.130-90_130-89insTGT	ENSP00000394413.1:n.130-90_130-89insTGT
ENST00000438045.5:c.130-90_130-89insTGT	ENSP00000410438.1:n.130-90_130-89insTGT
ENST00000484913.5:n.134-90_134-89insTGT
NM_000466.2:c.130-90_130-89insTGT	NP_000457.1:n.130-90_130-89insTGT
NM_001282677.1:c.130-90_130-89insTGT	NP_001269606.1:n.130-90_130-89insTGT
NM_001282678.1:c.-530-90_-530-89insTGT	NP_001269607.1:n.-530-90_-530-89insTGT
XR_242246.3:n.226-90_226-89insTGT
XR_242246.5:n.177-90_177-89insTGT
NM_000466.3:c.130-90_130-89insTGT MANE Select	NP_000457.1:n.130-90_130-89insTGT
NM_001282677.2:c.130-90_130-89insTGT	NP_001269606.1:n.130-90_130-89insTGT
NM_001282678.2:c.-530-90_-530-89insTGT	NP_001269607.1:n.-530-90_-530-89insTGT