Canonical Allele Identifier: CA368182926

Gene: PEX1

Linked Data

• MyVariant Identifiers: chr7:g.92134067G>T (hg19) ; chr7:g.92504753G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92504753G>T , CM000669.2:g.92504753G>T	GRCh38
NC_000007.13:g.92134067G>T , CM000669.1:g.92134067G>T	GRCh37
NC_000007.12:g.91972003G>T	NCBI36
NG_008341.1:g.28779C>A
NG_008341.2:g.28779C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000248633.9:c.2050C>A MANE Select	ENSP00000248633.4:p.Gln684Lys
ENST00000248633.8:c.2050C>A	ENSP00000248633.4:p.Gln684Lys
ENST00000428214.5:c.1900+1495C>A	ENSP00000394413.1:n.1900+1495C>A
ENST00000438045.5:c.1084C>A	ENSP00000410438.1:p.Gln362Lys
ENST00000484913.5:n.2089C>A
ENST00000496420.5:n.1726C>A
NM_000466.2:c.2050C>A	NP_000457.1:p.Gln684Lys
NM_001282677.1:c.1900+1495C>A	NP_001269606.1:n.1900+1495C>A
NM_001282678.1:c.1426C>A	NP_001269607.1:p.Gln476Lys
XM_005250433.3:c.301C>A	XP_005250490.1:p.Gln101Lys
XR_242246.3:n.2146C>A
XM_017012319.2:c.301C>A	XP_016867808.1:p.Gln101Lys
XR_001744808.2:n.1077C>A
XR_242246.5:n.2097C>A
NM_000466.3:c.2050C>A MANE Select	NP_000457.1:p.Gln684Lys
NM_001282677.2:c.1900+1495C>A	NP_001269606.1:n.1900+1495C>A
NM_001282678.2:c.1426C>A	NP_001269607.1:p.Gln476Lys