Canonical Allele Identifier: CA368198687

Gene: PEX1

Linked Data

• dbSNP Id: rs1792850948
• gnomAD v3: 7-92517535-C-G
• gnomAD v4: 7-92517535-C-G
• MyVariant Identifiers: chr7:g.92146849C>G (hg19) ; chr7:g.92517535C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92517535C>G , CM000669.2:g.92517535C>G	GRCh38
NC_000007.13:g.92146849C>G , CM000669.1:g.92146849C>G	GRCh37
NC_000007.12:g.91984785C>G	NCBI36
NG_008341.1:g.15997G>C
NG_008341.2:g.15997G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.980G>C MANE Select	ENSP00000248633.4:p.Ser327Thr
ENST00000248633.8:c.980G>C	ENSP00000248633.4:p.Ser327Thr
ENST00000428214.5:c.980G>C	ENSP00000394413.1:p.Ser327Thr
ENST00000438045.5:c.274-3568G>C	ENSP00000410438.1:n.274-3568G>C
ENST00000484913.5:n.1019G>C
NM_000466.2:c.980G>C	NP_000457.1:p.Ser327Thr
NM_001282677.1:c.980G>C	NP_001269606.1:p.Ser327Thr
NM_001282678.1:c.356G>C	NP_001269607.1:p.Ser119Thr
XR_242246.3:n.1076G>C
XM_017012319.2:c.-687G>C	XP_016867808.1:n.-687G>C
XR_001744808.2:n.90G>C
XR_242246.5:n.1027G>C
NM_000466.3:c.980G>C MANE Select	NP_000457.1:p.Ser327Thr
NM_001282677.2:c.980G>C	NP_001269606.1:p.Ser327Thr
NM_001282678.2:c.356G>C	NP_001269607.1:p.Ser119Thr