Canonical Allele Identifier: CA1725930652

Gene: PEX1 GATAD1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92493909_92493912delinsAATT , CM000669.2:g.92493909_92493912delinsAATT	GRCh38
NC_000007.13:g.92123223_92123226delinsAATT , CM000669.1:g.92123223_92123226delinsAATT	GRCh37
NC_000007.12:g.91961159_91961162delinsAATT	NCBI36
NG_008341.1:g.39620_39623delinsAATT
NG_008341.2:g.39620_39623delinsAATT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.3030+381_3030+384delinsAATT (PEX1) MANE Select	ENSP00000248633.4:n.3030+381_3030+384delinsAATT
ENST00000248633.8:c.3030+381_3030+384delinsAATT (PEX1)	ENSP00000248633.4:n.3030+381_3030+384delinsAATT
ENST00000428214.5:c.2859+381_2859+384delinsAATT (PEX1)	ENSP00000394413.1:n.2859+381_2859+384delinsAATT
ENST00000438045.5:c.2064+381_2064+384delinsAATT (PEX1)	ENSP00000410438.1:n.2064+381_2064+384delinsAATT
ENST00000484913.5:n.3069+381_3069+384delinsAATT (PEX1)
ENST00000496420.5:n.3303_3306delinsAATT (PEX1)
NM_000466.2:c.3030+381_3030+384delinsAATT (PEX1)	NP_000457.1:n.3030+381_3030+384delinsAATT
NM_001282677.1:c.2859+381_2859+384delinsAATT (PEX1)	NP_001269606.1:n.2859+381_2859+384delinsAATT
NM_001282678.1:c.2406+381_2406+384delinsAATT (PEX1)	NP_001269607.1:n.2406+381_2406+384delinsAATT
XM_005250433.3:c.1281+381_1281+384delinsAATT (PEX1)	XP_005250490.1:n.1281+381_1281+384delinsAATT
XR_242246.3:n.3126+381_3126+384delinsAATT (PEX1)
XM_017012319.2:c.1281+381_1281+384delinsAATT (PEX1)	XP_016867808.1:n.1281+381_1281+384delinsAATT
XR_001744808.2:n.2057+381_2057+384delinsAATT (PEX1)
XR_001744843.2:n.4878_4881delinsAATT (GATAD1)
XR_242246.5:n.3077+381_3077+384delinsAATT (PEX1)
XR_927494.3:n.3729_3732delinsAATT (GATAD1)
XR_927503.3:n.3660_3663delinsAATT (GATAD1)
NM_000466.3:c.3030+381_3030+384delinsAATT (PEX1) MANE Select	NP_000457.1:n.3030+381_3030+384delinsAATT
NM_001282677.2:c.2859+381_2859+384delinsAATT (PEX1)	NP_001269606.1:n.2859+381_2859+384delinsAATT
NM_001282678.2:c.2406+381_2406+384delinsAATT (PEX1)	NP_001269607.1:n.2406+381_2406+384delinsAATT