Canonical Allele Identifier: CA368182193

Gene: PEX1

Linked Data

• MyVariant Identifiers: chr7:g.92132496C>T (hg19) ; chr7:g.92503182C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92503182C>T , CM000669.2:g.92503182C>T	GRCh38
NC_000007.13:g.92132496C>T , CM000669.1:g.92132496C>T	GRCh37
NC_000007.12:g.91970432C>T	NCBI36
NG_008341.1:g.30350G>A
NG_008341.2:g.30350G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000248633.9:c.2085G>A MANE Select	ENSP00000248633.4:p.Met695Ile
ENST00000248633.8:c.2085G>A	ENSP00000248633.4:p.Met695Ile
ENST00000428214.5:c.1914G>A	ENSP00000394413.1:p.Met638Ile
ENST00000438045.5:c.1119G>A	ENSP00000410438.1:p.Met373Ile
ENST00000484913.5:n.2124G>A
ENST00000496420.5:n.1761G>A
NM_000466.2:c.2085G>A	NP_000457.1:p.Met695Ile
NM_001282677.1:c.1914G>A	NP_001269606.1:p.Met638Ile
NM_001282678.1:c.1461G>A	NP_001269607.1:p.Met487Ile
XM_005250433.3:c.336G>A	XP_005250490.1:p.Met112Ile
XR_242246.3:n.2181G>A
XM_017012319.2:c.336G>A	XP_016867808.1:p.Met112Ile
XR_001744808.2:n.1112G>A
XR_242246.5:n.2132G>A
NM_000466.3:c.2085G>A MANE Select	NP_000457.1:p.Met695Ile
NM_001282677.2:c.1914G>A	NP_001269606.1:p.Met638Ile
NM_001282678.2:c.1461G>A	NP_001269607.1:p.Met487Ile