Canonical Allele Identifier: CA368184000

Gene: PEX1

Linked Data

• MyVariant Identifiers: chr7:g.92134180A>G (hg19) ; chr7:g.92504866A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92504866A>G , CM000669.2:g.92504866A>G	GRCh38
NC_000007.13:g.92134180A>G , CM000669.1:g.92134180A>G	GRCh37
NC_000007.12:g.91972116A>G	NCBI36
NG_008341.1:g.28666T>C
NG_008341.2:g.28666T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000248633.9:c.1937T>C MANE Select	ENSP00000248633.4:p.Val646Ala
ENST00000248633.8:c.1937T>C	ENSP00000248633.4:p.Val646Ala
ENST00000428214.5:c.1900+1382T>C	ENSP00000394413.1:n.1900+1382T>C
ENST00000438045.5:c.971T>C	ENSP00000410438.1:p.Val324Ala
ENST00000484913.5:n.1976T>C
ENST00000496420.5:n.1613T>C
NM_000466.2:c.1937T>C	NP_000457.1:p.Val646Ala
NM_001282677.1:c.1900+1382T>C	NP_001269606.1:n.1900+1382T>C
NM_001282678.1:c.1313T>C	NP_001269607.1:p.Val438Ala
XM_005250433.3:c.188T>C	XP_005250490.1:p.Val63Ala
XR_242246.3:n.2033T>C
XM_017012319.2:c.188T>C	XP_016867808.1:p.Val63Ala
XR_001744808.2:n.964T>C
XR_242246.5:n.1984T>C
NM_000466.3:c.1937T>C MANE Select	NP_000457.1:p.Val646Ala
NM_001282677.2:c.1900+1382T>C	NP_001269606.1:n.1900+1382T>C
NM_001282678.2:c.1313T>C	NP_001269607.1:p.Val438Ala