Canonical Allele Identifier: CA368198395

Gene: PEX1

Linked Data

• dbSNP Id: rs1792846805
• gnomAD v3: 7-92517466-T-C
• gnomAD v4: 7-92517466-T-C
• MyVariant Identifiers: chr7:g.92146780T>C (hg19) ; chr7:g.92517466T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92517466T>C , CM000669.2:g.92517466T>C	GRCh38
NC_000007.13:g.92146780T>C , CM000669.1:g.92146780T>C	GRCh37
NC_000007.12:g.91984716T>C	NCBI36
NG_008341.1:g.16066A>G
NG_008341.2:g.16066A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.1049A>G MANE Select	ENSP00000248633.4:p.Gln350Arg
ENST00000248633.8:c.1049A>G	ENSP00000248633.4:p.Gln350Arg
ENST00000428214.5:c.1049A>G	ENSP00000394413.1:p.Gln350Arg
ENST00000438045.5:c.274-3499A>G	ENSP00000410438.1:n.274-3499A>G
ENST00000484913.5:n.1088A>G
NM_000466.2:c.1049A>G	NP_000457.1:p.Gln350Arg
NM_001282677.1:c.1049A>G	NP_001269606.1:p.Gln350Arg
NM_001282678.1:c.425A>G	NP_001269607.1:p.Gln142Arg
XR_242246.3:n.1145A>G
XM_017012319.2:c.-618A>G	XP_016867808.1:n.-618A>G
XR_001744808.2:n.159A>G
XR_242246.5:n.1096A>G
NM_000466.3:c.1049A>G MANE Select	NP_000457.1:p.Gln350Arg
NM_001282677.2:c.1049A>G	NP_001269606.1:p.Gln350Arg
NM_001282678.2:c.425A>G	NP_001269607.1:p.Gln142Arg