Canonical Allele Identifier: CA368183907

Gene: PEX1

Linked Data

• MyVariant Identifiers: chr7:g.92134172A>G (hg19) ; chr7:g.92504858A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92504858A>G , CM000669.2:g.92504858A>G	GRCh38
NC_000007.13:g.92134172A>G , CM000669.1:g.92134172A>G	GRCh37
NC_000007.12:g.91972108A>G	NCBI36
NG_008341.1:g.28674T>C
NG_008341.2:g.28674T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000248633.9:c.1945T>C MANE Select	ENSP00000248633.4:p.Ser649Pro
ENST00000248633.8:c.1945T>C	ENSP00000248633.4:p.Ser649Pro
ENST00000428214.5:c.1900+1390T>C	ENSP00000394413.1:n.1900+1390T>C
ENST00000438045.5:c.979T>C	ENSP00000410438.1:p.Ser327Pro
ENST00000484913.5:n.1984T>C
ENST00000496420.5:n.1621T>C
NM_000466.2:c.1945T>C	NP_000457.1:p.Ser649Pro
NM_001282677.1:c.1900+1390T>C	NP_001269606.1:n.1900+1390T>C
NM_001282678.1:c.1321T>C	NP_001269607.1:p.Ser441Pro
XM_005250433.3:c.196T>C	XP_005250490.1:p.Ser66Pro
XR_242246.3:n.2041T>C
XM_017012319.2:c.196T>C	XP_016867808.1:p.Ser66Pro
XR_001744808.2:n.972T>C
XR_242246.5:n.1992T>C
NM_000466.3:c.1945T>C MANE Select	NP_000457.1:p.Ser649Pro
NM_001282677.2:c.1900+1390T>C	NP_001269606.1:n.1900+1390T>C
NM_001282678.2:c.1321T>C	NP_001269607.1:p.Ser441Pro