Canonical Allele Identifier: CA368168482

Gene: PEX1 GATAD1

Linked Data

• MyVariant Identifiers: chr7:g.92123845A>G (hg19) ; chr7:g.92494531A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92494531A>G , CM000669.2:g.92494531A>G	GRCh38
NC_000007.13:g.92123845A>G , CM000669.1:g.92123845A>G	GRCh37
NC_000007.12:g.91961781A>G	NCBI36
NG_008341.1:g.39001T>C
NG_008341.2:g.39001T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000248633.9:c.2882T>C (PEX1) MANE Select	ENSP00000248633.4:p.Val961Ala
ENST00000248633.8:c.2882T>C (PEX1)	ENSP00000248633.4:p.Val961Ala
ENST00000428214.5:c.2711T>C (PEX1)	ENSP00000394413.1:p.Val904Ala
ENST00000438045.5:c.1916T>C (PEX1)	ENSP00000410438.1:p.Val639Ala
ENST00000484913.5:n.2921T>C (PEX1)
ENST00000496420.5:n.2774T>C (PEX1)
NM_000466.2:c.2882T>C (PEX1)	NP_000457.1:p.Val961Ala
NM_001282677.1:c.2711T>C (PEX1)	NP_001269606.1:p.Val904Ala
NM_001282678.1:c.2258T>C (PEX1)	NP_001269607.1:p.Val753Ala
XM_005250433.3:c.1133T>C (PEX1)	XP_005250490.1:p.Val378Ala
XR_242246.3:n.2978T>C (PEX1)
XM_017012319.2:c.1133T>C (PEX1)	XP_016867808.1:p.Val378Ala
XR_001744808.2:n.1909T>C (PEX1)
XR_001744843.2:n.5500A>G (GATAD1)
XR_242246.5:n.2929T>C (PEX1)
XR_927494.3:n.4351A>G (GATAD1)
XR_927503.3:n.4282A>G (GATAD1)
NM_000466.3:c.2882T>C (PEX1) MANE Select	NP_000457.1:p.Val961Ala
NM_001282677.2:c.2711T>C (PEX1)	NP_001269606.1:p.Val904Ala
NM_001282678.2:c.2258T>C (PEX1)	NP_001269607.1:p.Val753Ala