Canonical Allele Identifier: CA161974527

Gene: PEX1

Linked Data

• dbSNP Id: rs914671341
• gnomAD v3: 7-92518845-T-C
• gnomAD v4: 7-92518845-T-C
• MyVariant Identifiers: chr7:g.92148159T>C (hg19) ; chr7:g.92518845T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92518845T>C , CM000669.2:g.92518845T>C	GRCh38
NC_000007.13:g.92148159T>C , CM000669.1:g.92148159T>C	GRCh37
NC_000007.12:g.91986095T>C	NCBI36
NG_008341.1:g.14687A>G
NG_008341.2:g.14687A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000248633.9:c.357+150A>G MANE Select	ENSP00000248633.4:n.357+150A>G
ENST00000248633.8:c.357+150A>G	ENSP00000248633.4:n.357+150A>G
ENST00000428214.5:c.357+150A>G	ENSP00000394413.1:n.357+150A>G
ENST00000438045.5:c.273+3257A>G	ENSP00000410438.1:n.273+3257A>G
ENST00000484913.5:n.396+115A>G
NM_000466.2:c.357+150A>G	NP_000457.1:n.357+150A>G
NM_001282677.1:c.357+150A>G	NP_001269606.1:n.357+150A>G
NM_001282678.1:c.-268+115A>G	NP_001269607.1:n.-268+115A>G
XR_242246.3:n.453+150A>G
XR_242246.5:n.404+150A>G
NM_000466.3:c.357+150A>G MANE Select	NP_000457.1:n.357+150A>G
NM_001282677.2:c.357+150A>G	NP_001269606.1:n.357+150A>G
NM_001282678.2:c.-268+115A>G	NP_001269607.1:n.-268+115A>G