Canonical Allele Identifier: CA576706730

Gene: PEX1

Linked Data

• dbSNP Id: rs1229390025
• gnomAD v2: 7-92131436-A-G
• gnomAD v3: 7-92502122-A-G
• gnomAD v4: 7-92502122-A-G
• MyVariant Identifiers: chr7:g.92131436A>G (hg19) ; chr7:g.92502122A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92502122A>G , CM000669.2:g.92502122A>G	GRCh38
NC_000007.13:g.92131436A>G , CM000669.1:g.92131436A>G	GRCh37
NC_000007.12:g.91969372A>G	NCBI36
NG_008341.1:g.31410T>C
NG_008341.2:g.31410T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000248633.9:c.2227-43T>C MANE Select	ENSP00000248633.4:n.2227-43T>C
ENST00000248633.8:c.2227-43T>C	ENSP00000248633.4:n.2227-43T>C
ENST00000428214.5:c.2056-43T>C	ENSP00000394413.1:n.2056-43T>C
ENST00000438045.5:c.1261-43T>C	ENSP00000410438.1:n.1261-43T>C
ENST00000484913.5:n.2266-43T>C
ENST00000496092.1:n.25-43T>C
ENST00000496420.5:n.1903-43T>C
NM_000466.2:c.2227-43T>C	NP_000457.1:n.2227-43T>C
NM_001282677.1:c.2056-43T>C	NP_001269606.1:n.2056-43T>C
NM_001282678.1:c.1603-43T>C	NP_001269607.1:n.1603-43T>C
XM_005250433.3:c.478-43T>C	XP_005250490.1:n.478-43T>C
XR_242246.3:n.2323-43T>C
XM_017012319.2:c.478-43T>C	XP_016867808.1:n.478-43T>C
XR_001744808.2:n.1254-43T>C
XR_242246.5:n.2274-43T>C
NM_000466.3:c.2227-43T>C MANE Select	NP_000457.1:n.2227-43T>C
NM_001282677.2:c.2056-43T>C	NP_001269606.1:n.2056-43T>C
NM_001282678.2:c.1603-43T>C	NP_001269607.1:n.1603-43T>C