Canonical Allele Identifier: CA456483740

Gene: PEX1

Linked Data

• dbSNP Id: rs1172220526
• gnomAD v2: 7-92140339-A-G
• gnomAD v4: 7-92511025-A-G
• MyVariant Identifiers: chr7:g.92140339A>G (hg19) ; chr7:g.92511025A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92511025A>G , CM000669.2:g.92511025A>G	GRCh38
NC_000007.13:g.92140339A>G , CM000669.1:g.92140339A>G	GRCh37
NC_000007.12:g.91978275A>G	NCBI36
NG_008341.1:g.22507T>C
NG_008341.2:g.22507T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000248633.9:c.1506T>C MANE Select	ENSP00000248633.4:p.Ser502=
ENST00000248633.8:c.1506T>C	ENSP00000248633.4:p.Ser502=
ENST00000422866.1:c.407T>C
ENST00000428214.5:c.1506T>C	ENSP00000394413.1:p.Ser502=
ENST00000438045.5:c.540T>C	ENSP00000410438.1:p.Ser180=
ENST00000476923.1:n.267T>C
ENST00000484913.5:n.1545T>C
NM_000466.2:c.1506T>C	NP_000457.1:p.Ser502=
NM_001282677.1:c.1506T>C	NP_001269606.1:p.Ser502=
NM_001282678.1:c.882T>C	NP_001269607.1:p.Ser294=
XM_005250433.3:c.-161T>C	XP_005250490.1:n.-161T>C
XR_242246.3:n.1602T>C
XM_017012319.2:c.-161T>C	XP_016867808.1:n.-161T>C
XR_001744808.2:n.616T>C
XR_242246.5:n.1553T>C
NM_000466.3:c.1506T>C MANE Select	NP_000457.1:p.Ser502=
NM_001282677.2:c.1506T>C	NP_001269606.1:p.Ser502=
NM_001282678.2:c.882T>C	NP_001269607.1:p.Ser294=