Canonical Allele Identifier: CA1104469515
Gene: PEX1 HGNC NCBI

Linked Data

gnomAD v3: 7-92506409-G-A
gnomAD v4: 7-92506409-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92506409G>A , CM000669.2:g.92506409G>A GRCh38
NC_000007.13:g.92135723G>A , CM000669.1:g.92135723G>A GRCh37
NC_000007.12:g.91973659G>A NCBI36
NG_008341.1:g.27123C>T
NG_008341.2:g.27123C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.1804-65C>T MANE Select ENSP00000248633.4:n.1804-65C>T
ENST00000248633.8:c.1804-65C>T ENSP00000248633.4:n.1804-65C>T
ENST00000422866.1:c.622-65C>T
ENST00000428214.5:c.1804-65C>T ENSP00000394413.1:n.1804-65C>T
ENST00000438045.5:c.838-65C>T ENSP00000410438.1:n.838-65C>T
ENST00000484913.5:n.1843-65C>T
ENST00000496420.5:n.1415C>T
NM_000466.2:c.1804-65C>T NP_000457.1:n.1804-65C>T
NM_001282677.1:c.1804-65C>T NP_001269606.1:n.1804-65C>T
NM_001282678.1:c.1180-65C>T NP_001269607.1:n.1180-65C>T
XM_005250433.3:c.55-65C>T XP_005250490.1:n.55-65C>T
XR_242246.3:n.1900-65C>T
XM_017012319.2:c.55-65C>T XP_016867808.1:n.55-65C>T
XR_001744808.2:n.831-65C>T
XR_242246.5:n.1851-65C>T
NM_000466.3:c.1804-65C>T MANE Select NP_000457.1:n.1804-65C>T
NM_001282677.2:c.1804-65C>T NP_001269606.1:n.1804-65C>T
NM_001282678.2:c.1180-65C>T NP_001269607.1:n.1180-65C>T