Canonical Allele Identifier: CA2776947699

Gene: PEX1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92522350_92522351insACT , CM000669.2:g.92522350_92522351insACT	GRCh38
NC_000007.13:g.92151664_92151665insACT , CM000669.1:g.92151664_92151665insACT	GRCh37
NC_000007.12:g.91989600_91989601insACT	NCBI36
NG_008341.1:g.11181_11182insAGT
NG_008341.2:g.11181_11182insAGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.130-106_130-105insAGT MANE Select	ENSP00000248633.4:n.130-106_130-105insAGT
ENST00000248633.8:c.130-106_130-105insAGT	ENSP00000248633.4:n.130-106_130-105insAGT
ENST00000428214.5:c.130-106_130-105insAGT	ENSP00000394413.1:n.130-106_130-105insAGT
ENST00000438045.5:c.130-106_130-105insAGT	ENSP00000410438.1:n.130-106_130-105insAGT
ENST00000484913.5:n.134-106_134-105insAGT
NM_000466.2:c.130-106_130-105insAGT	NP_000457.1:n.130-106_130-105insAGT
NM_001282677.1:c.130-106_130-105insAGT	NP_001269606.1:n.130-106_130-105insAGT
NM_001282678.1:c.-530-106_-530-105insAGT	NP_001269607.1:n.-530-106_-530-105insAGT
XR_242246.3:n.226-106_226-105insAGT
XR_242246.5:n.177-106_177-105insAGT
NM_000466.3:c.130-106_130-105insAGT MANE Select	NP_000457.1:n.130-106_130-105insAGT
NM_001282677.2:c.130-106_130-105insAGT	NP_001269606.1:n.130-106_130-105insAGT
NM_001282678.2:c.-530-106_-530-105insAGT	NP_001269607.1:n.-530-106_-530-105insAGT