Canonical Allele Identifier: CA161956772

Gene: PEX1

Linked Data

• dbSNP Id: rs1003207203
• gnomAD v3: 7-92496410-A-G
• gnomAD v4: 7-92496410-A-G
• MyVariant Identifiers: chr7:g.92125724A>G (hg19) ; chr7:g.92496410A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92496410A>G , CM000669.2:g.92496410A>G	GRCh38
NC_000007.13:g.92125724A>G , CM000669.1:g.92125724A>G	GRCh37
NC_000007.12:g.91963660A>G	NCBI36
NG_008341.1:g.37122T>C
NG_008341.2:g.37122T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.2783+303T>C MANE Select	ENSP00000248633.4:n.2783+303T>C
ENST00000248633.8:c.2783+303T>C	ENSP00000248633.4:n.2783+303T>C
ENST00000428214.5:c.2612+303T>C	ENSP00000394413.1:n.2612+303T>C
ENST00000438045.5:c.1817+303T>C	ENSP00000410438.1:n.1817+303T>C
ENST00000484913.5:n.2822+303T>C
ENST00000496420.5:n.2675+303T>C
NM_000466.2:c.2783+303T>C	NP_000457.1:n.2783+303T>C
NM_001282677.1:c.2612+303T>C	NP_001269606.1:n.2612+303T>C
NM_001282678.1:c.2159+303T>C	NP_001269607.1:n.2159+303T>C
XM_005250433.3:c.1034+303T>C	XP_005250490.1:n.1034+303T>C
XR_242246.3:n.2879+303T>C
XM_017012319.2:c.1034+303T>C	XP_016867808.1:n.1034+303T>C
XR_001744808.2:n.1810+303T>C
XR_242246.5:n.2830+303T>C
NM_000466.3:c.2783+303T>C MANE Select	NP_000457.1:n.2783+303T>C
NM_001282677.2:c.2612+303T>C	NP_001269606.1:n.2612+303T>C
NM_001282678.2:c.2159+303T>C	NP_001269607.1:n.2159+303T>C