Canonical Allele Identifier: CA368174033

Gene: PEX1

Linked Data

• MyVariant Identifiers: chr7:g.92129115C>G (hg19) ; chr7:g.92499801C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92499801C>G , CM000669.2:g.92499801C>G	GRCh38
NC_000007.13:g.92129115C>G , CM000669.1:g.92129115C>G	GRCh37
NC_000007.12:g.91967051C>G	NCBI36
NG_008341.1:g.33731G>C
NG_008341.2:g.33731G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.2621G>C MANE Select	ENSP00000248633.4:p.Arg874Thr
ENST00000248633.8:c.2621G>C	ENSP00000248633.4:p.Arg874Thr
ENST00000428214.5:c.2450G>C	ENSP00000394413.1:p.Arg817Thr
ENST00000438045.5:c.1655G>C	ENSP00000410438.1:p.Arg552Thr
ENST00000484913.5:n.2660G>C
ENST00000496420.5:n.2513G>C
NM_000466.2:c.2621G>C	NP_000457.1:p.Arg874Thr
NM_001282677.1:c.2450G>C	NP_001269606.1:p.Arg817Thr
NM_001282678.1:c.1997G>C	NP_001269607.1:p.Arg666Thr
XM_005250433.3:c.872G>C	XP_005250490.1:p.Arg291Thr
XR_242246.3:n.2717G>C
XM_017012319.2:c.872G>C	XP_016867808.1:p.Arg291Thr
XR_001744808.2:n.1648G>C
XR_242246.5:n.2668G>C
NM_000466.3:c.2621G>C MANE Select	NP_000457.1:p.Arg874Thr
NM_001282677.2:c.2450G>C	NP_001269606.1:p.Arg817Thr
NM_001282678.2:c.1997G>C	NP_001269607.1:p.Arg666Thr