Canonical Allele Identifier: CA368200817

Gene: PEX1

Linked Data

• dbSNP Id: rs757244597
• gnomAD v3: 7-92517886-A-T
• gnomAD v4: 7-92517886-A-T
• MyVariant Identifiers: chr7:g.92147200A>T (hg19) ; chr7:g.92517886A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92517886A>T , CM000669.2:g.92517886A>T	GRCh38
NC_000007.13:g.92147200A>T , CM000669.1:g.92147200A>T	GRCh37
NC_000007.12:g.91985136A>T	NCBI36
NG_008341.1:g.15646T>A
NG_008341.2:g.15646T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.629T>A MANE Select	ENSP00000248633.4:p.Met210Lys
ENST00000248633.8:c.629T>A	ENSP00000248633.4:p.Met210Lys
ENST00000428214.5:c.629T>A	ENSP00000394413.1:p.Met210Lys
ENST00000438045.5:c.274-3919T>A	ENSP00000410438.1:n.274-3919T>A
ENST00000484913.5:n.668T>A
NM_000466.2:c.629T>A	NP_000457.1:p.Met210Lys
NM_001282677.1:c.629T>A	NP_001269606.1:p.Met210Lys
NM_001282678.1:c.5T>A	NP_001269607.1:p.Met2Lys
XR_242246.3:n.725T>A
XR_242246.5:n.676T>A
NM_000466.3:c.629T>A MANE Select	NP_000457.1:p.Met210Lys
NM_001282677.2:c.629T>A	NP_001269606.1:p.Met210Lys
NM_001282678.2:c.5T>A	NP_001269607.1:p.Met2Lys