Canonical Allele Identifier: CA4341600

Gene: PEX1

Linked Data

• dbSNP Id: rs769516058
• ExAC: 7:92147430 C / G
• gnomAD v2: 7-92147430-C-G
• gnomAD v3: 7-92518116-C-G
• gnomAD v4: 7-92518116-C-G
• MyVariant Identifiers: chr7:g.92147430C>G (hg19) ; chr7:g.92518116C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92518116C>G , CM000669.2:g.92518116C>G	GRCh38
NC_000007.13:g.92147430C>G , CM000669.1:g.92147430C>G	GRCh37
NC_000007.12:g.91985366C>G	NCBI36
NG_008341.1:g.15416G>C
NG_008341.2:g.15416G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.472+25G>C MANE Select	ENSP00000248633.4:n.472+25G>C
ENST00000248633.8:c.472+25G>C	ENSP00000248633.4:n.472+25G>C
ENST00000428214.5:c.472+25G>C	ENSP00000394413.1:n.472+25G>C
ENST00000438045.5:c.273+3986G>C	ENSP00000410438.1:n.273+3986G>C
ENST00000484913.5:n.511+25G>C
NM_000466.2:c.472+25G>C	NP_000457.1:n.472+25G>C
NM_001282677.1:c.472+25G>C	NP_001269606.1:n.472+25G>C
NM_001282678.1:c.-153+25G>C	NP_001269607.1:n.-153+25G>C
XR_242246.3:n.568+25G>C
XR_242246.5:n.519+25G>C
NM_000466.3:c.472+25G>C MANE Select	NP_000457.1:n.472+25G>C
NM_001282677.2:c.472+25G>C	NP_001269606.1:n.472+25G>C
NM_001282678.2:c.-153+25G>C	NP_001269607.1:n.-153+25G>C