Canonical Allele Identifier: CA456483500

Gene: PEX1

Linked Data

• MyVariant Identifiers: chr7:g.92135632T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92506318T>C , CM000669.2:g.92506318T>C	GRCh38
NC_000007.13:g.92135632T>C , CM000669.1:g.92135632T>C	GRCh37
NC_000007.12:g.91973568T>C	NCBI36
NG_008341.1:g.27214A>G
NG_008341.2:g.27214A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000248633.9:c.1830A>G MANE Select	ENSP00000248633.4:p.Lys610=
ENST00000248633.8:c.1830A>G	ENSP00000248633.4:p.Lys610=
ENST00000422866.1:c.648A>G
ENST00000428214.5:c.1830A>G	ENSP00000394413.1:p.Lys610=
ENST00000438045.5:c.864A>G	ENSP00000410438.1:p.Lys288=
ENST00000484913.5:n.1869A>G
ENST00000496420.5:n.1506A>G
NM_000466.2:c.1830A>G	NP_000457.1:p.Lys610=
NM_001282677.1:c.1830A>G	NP_001269606.1:p.Lys610=
NM_001282678.1:c.1206A>G	NP_001269607.1:p.Lys402=
XM_005250433.3:c.81A>G	XP_005250490.1:p.Lys27=
XR_242246.3:n.1926A>G
XM_017012319.2:c.81A>G	XP_016867808.1:p.Lys27=
XR_001744808.2:n.857A>G
XR_242246.5:n.1877A>G
NM_000466.3:c.1830A>G MANE Select	NP_000457.1:p.Lys610=
NM_001282677.2:c.1830A>G	NP_001269606.1:p.Lys610=
NM_001282678.2:c.1206A>G	NP_001269607.1:p.Lys402=