Canonical Allele Identifier: CA368183747

Gene: PEX1

Linked Data

• dbSNP Id: rs1792105509
• MyVariant Identifiers: chr7:g.92134156A>G (hg19) ; chr7:g.92504842A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92504842A>G , CM000669.2:g.92504842A>G	GRCh38
NC_000007.13:g.92134156A>G , CM000669.1:g.92134156A>G	GRCh37
NC_000007.12:g.91972092A>G	NCBI36
NG_008341.1:g.28690T>C
NG_008341.2:g.28690T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.1961T>C MANE Select	ENSP00000248633.4:p.Met654Thr
ENST00000248633.8:c.1961T>C	ENSP00000248633.4:p.Met654Thr
ENST00000428214.5:c.1900+1406T>C	ENSP00000394413.1:n.1900+1406T>C
ENST00000438045.5:c.995T>C	ENSP00000410438.1:p.Met332Thr
ENST00000484913.5:n.2000T>C
ENST00000496420.5:n.1637T>C
NM_000466.2:c.1961T>C	NP_000457.1:p.Met654Thr
NM_001282677.1:c.1900+1406T>C	NP_001269606.1:n.1900+1406T>C
NM_001282678.1:c.1337T>C	NP_001269607.1:p.Met446Thr
XM_005250433.3:c.212T>C	XP_005250490.1:p.Met71Thr
XR_242246.3:n.2057T>C
XM_017012319.2:c.212T>C	XP_016867808.1:p.Met71Thr
XR_001744808.2:n.988T>C
XR_242246.5:n.2008T>C
NM_000466.3:c.1961T>C MANE Select	NP_000457.1:p.Met654Thr
NM_001282677.2:c.1900+1406T>C	NP_001269606.1:n.1900+1406T>C
NM_001282678.2:c.1337T>C	NP_001269607.1:p.Met446Thr