Canonical Allele Identifier: CA368200566

Gene: PEX1

Linked Data

• dbSNP Id: rs749874311
• gnomAD v2: 7-92147158-C-A
• gnomAD v4: 7-92517844-C-A
• MyVariant Identifiers: chr7:g.92147158C>A (hg19) ; chr7:g.92517844C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92517844C>A , CM000669.2:g.92517844C>A	GRCh38
NC_000007.13:g.92147158C>A , CM000669.1:g.92147158C>A	GRCh37
NC_000007.12:g.91985094C>A	NCBI36
NG_008341.1:g.15688G>T
NG_008341.2:g.15688G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.671G>T MANE Select	ENSP00000248633.4:p.Gly224Val
ENST00000248633.8:c.671G>T	ENSP00000248633.4:p.Gly224Val
ENST00000428214.5:c.671G>T	ENSP00000394413.1:p.Gly224Val
ENST00000438045.5:c.274-3877G>T	ENSP00000410438.1:n.274-3877G>T
ENST00000484913.5:n.710G>T
NM_000466.2:c.671G>T	NP_000457.1:p.Gly224Val
NM_001282677.1:c.671G>T	NP_001269606.1:p.Gly224Val
NM_001282678.1:c.47G>T	NP_001269607.1:p.Gly16Val
XR_242246.3:n.767G>T
XR_242246.5:n.718G>T
NM_000466.3:c.671G>T MANE Select	NP_000457.1:p.Gly224Val
NM_001282677.2:c.671G>T	NP_001269606.1:p.Gly224Val
NM_001282678.2:c.47G>T	NP_001269607.1:p.Gly16Val