Canonical Allele Identifier: CA456624397

Gene: PEX1

Linked Data

• MyVariant Identifiers: chr7:g.92146911A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92517597A>G , CM000669.2:g.92517597A>G	GRCh38
NC_000007.13:g.92146911A>G , CM000669.1:g.92146911A>G	GRCh37
NC_000007.12:g.91984847A>G	NCBI36
NG_008341.1:g.15935T>C
NG_008341.2:g.15935T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000248633.9:c.918T>C MANE Select	ENSP00000248633.4:p.Phe306=
ENST00000248633.8:c.918T>C	ENSP00000248633.4:p.Phe306=
ENST00000428214.5:c.918T>C	ENSP00000394413.1:p.Phe306=
ENST00000438045.5:c.274-3630T>C	ENSP00000410438.1:n.274-3630T>C
ENST00000484913.5:n.957T>C
NM_000466.2:c.918T>C	NP_000457.1:p.Phe306=
NM_001282677.1:c.918T>C	NP_001269606.1:p.Phe306=
NM_001282678.1:c.294T>C	NP_001269607.1:p.Phe98=
XR_242246.3:n.1014T>C
XM_017012319.2:c.-749T>C	XP_016867808.1:n.-749T>C
XR_001744808.2:n.28T>C
XR_242246.5:n.965T>C
NM_000466.3:c.918T>C MANE Select	NP_000457.1:p.Phe306=
NM_001282677.2:c.918T>C	NP_001269606.1:p.Phe306=
NM_001282678.2:c.294T>C	NP_001269607.1:p.Phe98=