Canonical Allele Identifier: CA368181112

Gene: PEX1

Linked Data

• MyVariant Identifiers: chr7:g.92132368T>G (hg19) ; chr7:g.92503054T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92503054T>G , CM000669.2:g.92503054T>G	GRCh38
NC_000007.13:g.92132368T>G , CM000669.1:g.92132368T>G	GRCh37
NC_000007.12:g.91970304T>G	NCBI36
NG_008341.1:g.30478A>C
NG_008341.2:g.30478A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.2213A>C MANE Select	ENSP00000248633.4:p.Gln738Pro
ENST00000248633.8:c.2213A>C	ENSP00000248633.4:p.Gln738Pro
ENST00000428214.5:c.2042A>C	ENSP00000394413.1:p.Gln681Pro
ENST00000438045.5:c.1247A>C	ENSP00000410438.1:p.Gln416Pro
ENST00000484913.5:n.2252A>C
ENST00000496092.1:n.11A>C
ENST00000496420.5:n.1889A>C
NM_000466.2:c.2213A>C	NP_000457.1:p.Gln738Pro
NM_001282677.1:c.2042A>C	NP_001269606.1:p.Gln681Pro
NM_001282678.1:c.1589A>C	NP_001269607.1:p.Gln530Pro
XM_005250433.3:c.464A>C	XP_005250490.1:p.Gln155Pro
XR_242246.3:n.2309A>C
XM_017012319.2:c.464A>C	XP_016867808.1:p.Gln155Pro
XR_001744808.2:n.1240A>C
XR_242246.5:n.2260A>C
NM_000466.3:c.2213A>C MANE Select	NP_000457.1:p.Gln738Pro
NM_001282677.2:c.2042A>C	NP_001269606.1:p.Gln681Pro
NM_001282678.2:c.1589A>C	NP_001269607.1:p.Gln530Pro