Canonical Allele Identifier: CA368185531

Gene: PEX1

Linked Data

• dbSNP Id: rs1157466034
• gnomAD v2: 7-92135654-C-G
• gnomAD v4: 7-92506340-C-G
• MyVariant Identifiers: chr7:g.92135654C>G (hg19) ; chr7:g.92506340C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92506340C>G , CM000669.2:g.92506340C>G	GRCh38
NC_000007.13:g.92135654C>G , CM000669.1:g.92135654C>G	GRCh37
NC_000007.12:g.91973590C>G	NCBI36
NG_008341.1:g.27192G>C
NG_008341.2:g.27192G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.1808G>C MANE Select	ENSP00000248633.4:p.Ser603Thr
ENST00000248633.8:c.1808G>C	ENSP00000248633.4:p.Ser603Thr
ENST00000422866.1:c.626G>C
ENST00000428214.5:c.1808G>C	ENSP00000394413.1:p.Ser603Thr
ENST00000438045.5:c.842G>C	ENSP00000410438.1:p.Ser281Thr
ENST00000484913.5:n.1847G>C
ENST00000496420.5:n.1484G>C
NM_000466.2:c.1808G>C	NP_000457.1:p.Ser603Thr
NM_001282677.1:c.1808G>C	NP_001269606.1:p.Ser603Thr
NM_001282678.1:c.1184G>C	NP_001269607.1:p.Ser395Thr
XM_005250433.3:c.59G>C	XP_005250490.1:p.Ser20Thr
XR_242246.3:n.1904G>C
XM_017012319.2:c.59G>C	XP_016867808.1:p.Ser20Thr
XR_001744808.2:n.835G>C
XR_242246.5:n.1855G>C
NM_000466.3:c.1808G>C MANE Select	NP_000457.1:p.Ser603Thr
NM_001282677.2:c.1808G>C	NP_001269606.1:p.Ser603Thr
NM_001282678.2:c.1184G>C	NP_001269607.1:p.Ser395Thr