Canonical Allele Identifier: CA368196904

Gene: PEX1

Linked Data

• MyVariant Identifiers: chr7:g.92146591C>G (hg19) ; chr7:g.92517277C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92517277C>G , CM000669.2:g.92517277C>G	GRCh38
NC_000007.13:g.92146591C>G , CM000669.1:g.92146591C>G	GRCh37
NC_000007.12:g.91984527C>G	NCBI36
NG_008341.1:g.16255G>C
NG_008341.2:g.16255G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.1238G>C MANE Select	ENSP00000248633.4:p.Trp413Ser
ENST00000248633.8:c.1238G>C	ENSP00000248633.4:p.Trp413Ser
ENST00000422866.1:c.139G>C
ENST00000428214.5:c.1238G>C	ENSP00000394413.1:p.Trp413Ser
ENST00000438045.5:c.274-3310G>C	ENSP00000410438.1:n.274-3310G>C
ENST00000484913.5:n.1277G>C
NM_000466.2:c.1238G>C	NP_000457.1:p.Trp413Ser
NM_001282677.1:c.1238G>C	NP_001269606.1:p.Trp413Ser
NM_001282678.1:c.614G>C	NP_001269607.1:p.Trp205Ser
XR_242246.3:n.1334G>C
XM_017012319.2:c.-429G>C	XP_016867808.1:n.-429G>C
XR_001744808.2:n.348G>C
XR_242246.5:n.1285G>C
NM_000466.3:c.1238G>C MANE Select	NP_000457.1:p.Trp413Ser
NM_001282677.2:c.1238G>C	NP_001269606.1:p.Trp413Ser
NM_001282678.2:c.614G>C	NP_001269607.1:p.Trp205Ser