Canonical Allele Identifier: CA843847706

Gene: PEX1

Linked Data

• dbSNP Id: rs1260087644
• gnomAD v3: 7-92502936-TC-T
• gnomAD v4: 7-92502936-TC-T
• MyVariant Identifiers: chr7:g.92132251del (hg19) ; chr7:g.92502937del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92502937del , CM000669.2:g.92502937del	GRCh38
NC_000007.13:g.92132251del , CM000669.1:g.92132251del	GRCh37
NC_000007.12:g.91970187del	NCBI36
NG_008341.1:g.30595del
NG_008341.2:g.30595del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.2226+104del MANE Select	ENSP00000248633.4:n.2226+104del
ENST00000248633.8:c.2226+104del	ENSP00000248633.4:n.2226+104del
ENST00000428214.5:c.2055+104del	ENSP00000394413.1:n.2055+104del
ENST00000438045.5:c.1260+104del	ENSP00000410438.1:n.1260+104del
ENST00000484913.5:n.2265+104del
ENST00000496092.1:n.24+104del
ENST00000496420.5:n.1902+104del
NM_000466.2:c.2226+104del	NP_000457.1:n.2226+104del
NM_001282677.1:c.2055+104del	NP_001269606.1:n.2055+104del
NM_001282678.1:c.1602+104del	NP_001269607.1:n.1602+104del
XM_005250433.3:c.477+104del	XP_005250490.1:n.477+104del
XR_242246.3:n.2322+104del
XM_017012319.2:c.477+104del	XP_016867808.1:n.477+104del
XR_001744808.2:n.1253+104del
XR_242246.5:n.2273+104del
NM_000466.3:c.2226+104del MANE Select	NP_000457.1:n.2226+104del
NM_001282677.2:c.2055+104del	NP_001269606.1:n.2055+104del
NM_001282678.2:c.1602+104del	NP_001269607.1:n.1602+104del