Canonical Allele Identifier: CA368190306

Gene: PEX1

Linked Data

• dbSNP Id: rs1418412029
• gnomAD v2: 7-92140337-A-G
• gnomAD v4: 7-92511023-A-G
• MyVariant Identifiers: chr7:g.92140337A>G (hg19) ; chr7:g.92511023A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92511023A>G , CM000669.2:g.92511023A>G	GRCh38
NC_000007.13:g.92140337A>G , CM000669.1:g.92140337A>G	GRCh37
NC_000007.12:g.91978273A>G	NCBI36
NG_008341.1:g.22509T>C
NG_008341.2:g.22509T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000248633.9:c.1508T>C MANE Select	ENSP00000248633.4:p.Ile503Thr
ENST00000248633.8:c.1508T>C	ENSP00000248633.4:p.Ile503Thr
ENST00000422866.1:c.409T>C
ENST00000428214.5:c.1508T>C	ENSP00000394413.1:p.Ile503Thr
ENST00000438045.5:c.542T>C	ENSP00000410438.1:p.Ile181Thr
ENST00000476923.1:n.269T>C
ENST00000484913.5:n.1547T>C
NM_000466.2:c.1508T>C	NP_000457.1:p.Ile503Thr
NM_001282677.1:c.1508T>C	NP_001269606.1:p.Ile503Thr
NM_001282678.1:c.884T>C	NP_001269607.1:p.Ile295Thr
XM_005250433.3:c.-159T>C	XP_005250490.1:n.-159T>C
XR_242246.3:n.1604T>C
XM_017012319.2:c.-159T>C	XP_016867808.1:n.-159T>C
XR_001744808.2:n.618T>C
XR_242246.5:n.1555T>C
NM_000466.3:c.1508T>C MANE Select	NP_000457.1:p.Ile503Thr
NM_001282677.2:c.1508T>C	NP_001269606.1:p.Ile503Thr
NM_001282678.2:c.884T>C	NP_001269607.1:p.Ile295Thr