Canonical Allele Identifier: CA368167310

Linked Data

dbSNP Id: rs1321349607
gnomAD v2: 7-92123620-G-A
gnomAD v3: 7-92494306-G-A
gnomAD v4: 7-92494306-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92494306G>A , CM000669.2:g.92494306G>A GRCh38
NC_000007.13:g.92123620G>A , CM000669.1:g.92123620G>A GRCh37
NC_000007.12:g.91961556G>A NCBI36
NG_008341.1:g.39226C>T
NG_008341.2:g.39226C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.3017C>T (PEX1) MANE Select ENSP00000248633.4:p.Pro1006Leu
ENST00000248633.8:c.3017C>T (PEX1) ENSP00000248633.4:p.Pro1006Leu
ENST00000428214.5:c.2846C>T (PEX1) ENSP00000394413.1:p.Pro949Leu
ENST00000438045.5:c.2051C>T (PEX1) ENSP00000410438.1:p.Pro684Leu
ENST00000484913.5:n.3056C>T (PEX1)
ENST00000496420.5:n.2909C>T (PEX1)
NM_000466.2:c.3017C>T (PEX1) NP_000457.1:p.Pro1006Leu
NM_001282677.1:c.2846C>T (PEX1) NP_001269606.1:p.Pro949Leu
NM_001282678.1:c.2393C>T (PEX1) NP_001269607.1:p.Pro798Leu
XM_005250433.3:c.1268C>T (PEX1) XP_005250490.1:p.Pro423Leu
XR_242246.3:n.3113C>T (PEX1)
XM_017012319.2:c.1268C>T (PEX1) XP_016867808.1:p.Pro423Leu
XR_001744808.2:n.2044C>T (PEX1)
XR_001744843.2:n.5275G>A (GATAD1)
XR_242246.5:n.3064C>T (PEX1)
XR_927494.3:n.4126G>A (GATAD1)
XR_927503.3:n.4057G>A (GATAD1)
NM_000466.3:c.3017C>T (PEX1) MANE Select NP_000457.1:p.Pro1006Leu
NM_001282677.2:c.2846C>T (PEX1) NP_001269606.1:p.Pro949Leu
NM_001282678.2:c.2393C>T (PEX1) NP_001269607.1:p.Pro798Leu