Canonical Allele Identifier: CA368196936

Gene: PEX1

Linked Data

• MyVariant Identifiers: chr7:g.92146594A>G (hg19) ; chr7:g.92517280A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92517280A>G , CM000669.2:g.92517280A>G	GRCh38
NC_000007.13:g.92146594A>G , CM000669.1:g.92146594A>G	GRCh37
NC_000007.12:g.91984530A>G	NCBI36
NG_008341.1:g.16252T>C
NG_008341.2:g.16252T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.1235T>C MANE Select	ENSP00000248633.4:p.Val412Ala
ENST00000248633.8:c.1235T>C	ENSP00000248633.4:p.Val412Ala
ENST00000422866.1:c.136T>C
ENST00000428214.5:c.1235T>C	ENSP00000394413.1:p.Val412Ala
ENST00000438045.5:c.274-3313T>C	ENSP00000410438.1:n.274-3313T>C
ENST00000484913.5:n.1274T>C
NM_000466.2:c.1235T>C	NP_000457.1:p.Val412Ala
NM_001282677.1:c.1235T>C	NP_001269606.1:p.Val412Ala
NM_001282678.1:c.611T>C	NP_001269607.1:p.Val204Ala
XR_242246.3:n.1331T>C
XM_017012319.2:c.-432T>C	XP_016867808.1:n.-432T>C
XR_001744808.2:n.345T>C
XR_242246.5:n.1282T>C
NM_000466.3:c.1235T>C MANE Select	NP_000457.1:p.Val412Ala
NM_001282677.2:c.1235T>C	NP_001269606.1:p.Val412Ala
NM_001282678.2:c.611T>C	NP_001269607.1:p.Val204Ala