Canonical Allele Identifier: CA161968610

Gene: PEX1

Linked Data

• dbSNP Id: rs1050047272
• gnomAD v4: 7-92511161-A-G
• MyVariant Identifiers: chr7:g.92140475A>G (hg19) ; chr7:g.92511161A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92511161A>G , CM000669.2:g.92511161A>G	GRCh38
NC_000007.13:g.92140475A>G , CM000669.1:g.92140475A>G	GRCh37
NC_000007.12:g.91978411A>G	NCBI36
NG_008341.1:g.22371T>C
NG_008341.2:g.22371T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.1484-114T>C MANE Select	ENSP00000248633.4:n.1484-114T>C
ENST00000248633.8:c.1484-114T>C	ENSP00000248633.4:n.1484-114T>C
ENST00000422866.1:c.385-114T>C
ENST00000428214.5:c.1484-114T>C	ENSP00000394413.1:n.1484-114T>C
ENST00000438045.5:c.518-114T>C	ENSP00000410438.1:n.518-114T>C
ENST00000476923.1:n.245-114T>C
ENST00000484913.5:n.1523-114T>C
NM_000466.2:c.1484-114T>C	NP_000457.1:n.1484-114T>C
NM_001282677.1:c.1484-114T>C	NP_001269606.1:n.1484-114T>C
NM_001282678.1:c.860-114T>C	NP_001269607.1:n.860-114T>C
XM_005250433.3:c.-183-114T>C	XP_005250490.1:n.-183-114T>C
XR_242246.3:n.1580-114T>C
XM_017012319.2:c.-183-114T>C	XP_016867808.1:n.-183-114T>C
XR_001744808.2:n.594-114T>C
XR_242246.5:n.1531-114T>C
NM_000466.3:c.1484-114T>C MANE Select	NP_000457.1:n.1484-114T>C
NM_001282677.2:c.1484-114T>C	NP_001269606.1:n.1484-114T>C
NM_001282678.2:c.860-114T>C	NP_001269607.1:n.860-114T>C