Canonical Allele Identifier: CA2776946800
Gene: PEX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92506449_92506459del , CM000669.2:g.92506449_92506459del GRCh38
NC_000007.13:g.92135763_92135773del , CM000669.1:g.92135763_92135773del GRCh37
NC_000007.12:g.91973699_91973709del NCBI36
NG_008341.1:g.27073_27083del
NG_008341.2:g.27073_27083del

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.1804-115_1804-105del MANE Select ENSP00000248633.4:n.1804-115_1804-105del
ENST00000248633.8:c.1804-115_1804-105del ENSP00000248633.4:n.1804-115_1804-105del
ENST00000422866.1:c.622-115_622-105del
ENST00000428214.5:c.1804-115_1804-105del ENSP00000394413.1:n.1804-115_1804-105del
ENST00000438045.5:c.838-115_838-105del ENSP00000410438.1:n.838-115_838-105del
ENST00000484913.5:n.1843-115_1843-105del
ENST00000496420.5:n.1365_1375del
NM_000466.2:c.1804-115_1804-105del NP_000457.1:n.1804-115_1804-105del
NM_001282677.1:c.1804-115_1804-105del NP_001269606.1:n.1804-115_1804-105del
NM_001282678.1:c.1180-115_1180-105del NP_001269607.1:n.1180-115_1180-105del
XM_005250433.3:c.55-115_55-105del XP_005250490.1:n.55-115_55-105del
XR_242246.3:n.1900-115_1900-105del
XM_017012319.2:c.55-115_55-105del XP_016867808.1:n.55-115_55-105del
XR_001744808.2:n.831-115_831-105del
XR_242246.5:n.1851-115_1851-105del
NM_000466.3:c.1804-115_1804-105del MANE Select NP_000457.1:n.1804-115_1804-105del
NM_001282677.2:c.1804-115_1804-105del NP_001269606.1:n.1804-115_1804-105del
NM_001282678.2:c.1180-115_1180-105del NP_001269607.1:n.1180-115_1180-105del