Canonical Allele Identifier: CA368174004

Gene: PEX1

Linked Data

• MyVariant Identifiers: chr7:g.92129112G>T (hg19) ; chr7:g.92499798G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92499798G>T , CM000669.2:g.92499798G>T	GRCh38
NC_000007.13:g.92129112G>T , CM000669.1:g.92129112G>T	GRCh37
NC_000007.12:g.91967048G>T	NCBI36
NG_008341.1:g.33734C>A
NG_008341.2:g.33734C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.2624C>A MANE Select	ENSP00000248633.4:p.Thr875Lys
ENST00000248633.8:c.2624C>A	ENSP00000248633.4:p.Thr875Lys
ENST00000428214.5:c.2453C>A	ENSP00000394413.1:p.Thr818Lys
ENST00000438045.5:c.1658C>A	ENSP00000410438.1:p.Thr553Lys
ENST00000484913.5:n.2663C>A
ENST00000496420.5:n.2516C>A
NM_000466.2:c.2624C>A	NP_000457.1:p.Thr875Lys
NM_001282677.1:c.2453C>A	NP_001269606.1:p.Thr818Lys
NM_001282678.1:c.2000C>A	NP_001269607.1:p.Thr667Lys
XM_005250433.3:c.875C>A	XP_005250490.1:p.Thr292Lys
XR_242246.3:n.2720C>A
XM_017012319.2:c.875C>A	XP_016867808.1:p.Thr292Lys
XR_001744808.2:n.1651C>A
XR_242246.5:n.2671C>A
NM_000466.3:c.2624C>A MANE Select	NP_000457.1:p.Thr875Lys
NM_001282677.2:c.2453C>A	NP_001269606.1:p.Thr818Lys
NM_001282678.2:c.2000C>A	NP_001269607.1:p.Thr667Lys