Canonical Allele Identifier: CA368197950

Gene: PEX1

Linked Data

• MyVariant Identifiers: chr7:g.92146710A>C (hg19) ; chr7:g.92517396A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92517396A>C , CM000669.2:g.92517396A>C	GRCh38
NC_000007.13:g.92146710A>C , CM000669.1:g.92146710A>C	GRCh37
NC_000007.12:g.91984646A>C	NCBI36
NG_008341.1:g.16136T>G
NG_008341.2:g.16136T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.1119T>G MANE Select	ENSP00000248633.4:p.Asp373Glu
ENST00000248633.8:c.1119T>G	ENSP00000248633.4:p.Asp373Glu
ENST00000422866.1:c.20T>G
ENST00000428214.5:c.1119T>G	ENSP00000394413.1:p.Asp373Glu
ENST00000438045.5:c.274-3429T>G	ENSP00000410438.1:n.274-3429T>G
ENST00000484913.5:n.1158T>G
NM_000466.2:c.1119T>G	NP_000457.1:p.Asp373Glu
NM_001282677.1:c.1119T>G	NP_001269606.1:p.Asp373Glu
NM_001282678.1:c.495T>G	NP_001269607.1:p.Asp165Glu
XR_242246.3:n.1215T>G
XM_017012319.2:c.-548T>G	XP_016867808.1:n.-548T>G
XR_001744808.2:n.229T>G
XR_242246.5:n.1166T>G
NM_000466.3:c.1119T>G MANE Select	NP_000457.1:p.Asp373Glu
NM_001282677.2:c.1119T>G	NP_001269606.1:p.Asp373Glu
NM_001282678.2:c.495T>G	NP_001269607.1:p.Asp165Glu