Canonical Allele Identifier: CA161963572

Gene: PEX1

Linked Data

• dbSNP Id: rs950106288
• MyVariant Identifiers: chr7:g.92132396G>C (hg19) ; chr7:g.92503082G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92503082G>C , CM000669.2:g.92503082G>C	GRCh38
NC_000007.13:g.92132396G>C , CM000669.1:g.92132396G>C	GRCh37
NC_000007.12:g.91970332G>C	NCBI36
NG_008341.1:g.30450C>G
NG_008341.2:g.30450C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000248633.9:c.2185C>G MANE Select	ENSP00000248633.4:p.His729Asp
ENST00000248633.8:c.2185C>G	ENSP00000248633.4:p.His729Asp
ENST00000428214.5:c.2014C>G	ENSP00000394413.1:p.His672Asp
ENST00000438045.5:c.1219C>G	ENSP00000410438.1:p.His407Asp
ENST00000484913.5:n.2224C>G
ENST00000496420.5:n.1861C>G
NM_000466.2:c.2185C>G	NP_000457.1:p.His729Asp
NM_001282677.1:c.2014C>G	NP_001269606.1:p.His672Asp
NM_001282678.1:c.1561C>G	NP_001269607.1:p.His521Asp
XM_005250433.3:c.436C>G	XP_005250490.1:p.His146Asp
XR_242246.3:n.2281C>G
XM_017012319.2:c.436C>G	XP_016867808.1:p.His146Asp
XR_001744808.2:n.1212C>G
XR_242246.5:n.2232C>G
NM_000466.3:c.2185C>G MANE Select	NP_000457.1:p.His729Asp
NM_001282677.2:c.2014C>G	NP_001269606.1:p.His672Asp
NM_001282678.2:c.1561C>G	NP_001269607.1:p.His521Asp