Canonical Allele Identifier: CA1104486731

Linked Data

dbSNP Id: rs1791332445
gnomAD v3: 7-92491659-G-A
gnomAD v4: 7-92491659-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92491659G>A , CM000669.2:g.92491659G>A GRCh38
NC_000007.13:g.92120973G>A , CM000669.1:g.92120973G>A GRCh37
NC_000007.12:g.91958909G>A NCBI36
NG_008341.1:g.41873C>T
NG_008341.2:g.41873C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.3208-157C>T (PEX1) MANE Select ENSP00000248633.4:n.3208-157C>T
ENST00000248633.8:c.3208-157C>T (PEX1) ENSP00000248633.4:n.3208-157C>T
ENST00000428214.5:c.3037-157C>T (PEX1) ENSP00000394413.1:n.3037-157C>T
ENST00000438045.5:c.2242-157C>T (PEX1) ENSP00000410438.1:n.2242-157C>T
ENST00000484913.5:n.3247-157C>T (PEX1)
ENST00000496420.5:n.4263-157C>T (PEX1)
NM_000466.2:c.3208-157C>T (PEX1) NP_000457.1:n.3208-157C>T
NM_001282677.1:c.3037-157C>T (PEX1) NP_001269606.1:n.3037-157C>T
NM_001282678.1:c.2584-157C>T (PEX1) NP_001269607.1:n.2584-157C>T
XM_005250433.3:c.1459-157C>T (PEX1) XP_005250490.1:n.1459-157C>T
XR_242246.3:n.3304-157C>T (PEX1)
XM_017012319.2:c.1459-157C>T (PEX1) XP_016867808.1:n.1459-157C>T
XR_001744808.2:n.2235-157C>T (PEX1)
XR_001744842.2:n.2697G>A (GATAD1)
XR_001744843.2:n.2628G>A (GATAD1)
XR_002956472.1:n.2754G>A (GATAD1)
XR_002956473.1:n.2785G>A (GATAD1)
XR_002956474.1:n.2702G>A (GATAD1)
XR_242246.5:n.3255-157C>T (PEX1)
XR_927494.3:n.1479G>A (GATAD1)
XR_927500.3:n.1476G>A (GATAD1)
XR_927503.3:n.1410G>A (GATAD1)
NM_000466.3:c.3208-157C>T (PEX1) MANE Select NP_000457.1:n.3208-157C>T
NM_001282677.2:c.3037-157C>T (PEX1) NP_001269606.1:n.3037-157C>T
NM_001282678.2:c.2584-157C>T (PEX1) NP_001269607.1:n.2584-157C>T