Canonical Allele Identifier: CA456483529

Gene: PEX1

Linked Data

• MyVariant Identifiers: chr7:g.92136314T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92507000T>G , CM000669.2:g.92507000T>G	GRCh38
NC_000007.13:g.92136314T>G , CM000669.1:g.92136314T>G	GRCh37
NC_000007.12:g.91974250T>G	NCBI36
NG_008341.1:g.26532A>C
NG_008341.2:g.26532A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.1797A>C MANE Select	ENSP00000248633.4:p.Gly599=
ENST00000248633.8:c.1797A>C	ENSP00000248633.4:p.Gly599=
ENST00000422866.1:c.615A>C
ENST00000428214.5:c.1797A>C	ENSP00000394413.1:p.Gly599=
ENST00000438045.5:c.831A>C	ENSP00000410438.1:p.Gly277=
ENST00000484913.5:n.1836A>C
ENST00000496420.5:n.824A>C
NM_000466.2:c.1797A>C	NP_000457.1:p.Gly599=
NM_001282677.1:c.1797A>C	NP_001269606.1:p.Gly599=
NM_001282678.1:c.1173A>C	NP_001269607.1:p.Gly391=
XM_005250433.3:c.48A>C	XP_005250490.1:p.Gly16=
XR_242246.3:n.1893A>C
XM_017012319.2:c.48A>C	XP_016867808.1:p.Gly16=
XR_001744808.2:n.824A>C
XR_242246.5:n.1844A>C
NM_000466.3:c.1797A>C MANE Select	NP_000457.1:p.Gly599=
NM_001282677.2:c.1797A>C	NP_001269606.1:p.Gly599=
NM_001282678.2:c.1173A>C	NP_001269607.1:p.Gly391=