Canonical Allele Identifier: CA2776946308

Gene: PEX1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92502169_92502172del , CM000669.2:g.92502169_92502172del	GRCh38
NC_000007.13:g.92131483_92131486del , CM000669.1:g.92131483_92131486del	GRCh37
NC_000007.12:g.91969419_91969422del	NCBI36
NG_008341.1:g.31362_31365del
NG_008341.2:g.31362_31365del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.2227-91_2227-88del MANE Select	ENSP00000248633.4:n.2227-91_2227-88del
ENST00000248633.8:c.2227-91_2227-88del	ENSP00000248633.4:n.2227-91_2227-88del
ENST00000428214.5:c.2056-91_2056-88del	ENSP00000394413.1:n.2056-91_2056-88del
ENST00000438045.5:c.1261-91_1261-88del	ENSP00000410438.1:n.1261-91_1261-88del
ENST00000484913.5:n.2266-91_2266-88del
ENST00000496092.1:n.25-91_25-88del
ENST00000496420.5:n.1903-91_1903-88del
NM_000466.2:c.2227-91_2227-88del	NP_000457.1:n.2227-91_2227-88del
NM_001282677.1:c.2056-91_2056-88del	NP_001269606.1:n.2056-91_2056-88del
NM_001282678.1:c.1603-91_1603-88del	NP_001269607.1:n.1603-91_1603-88del
XM_005250433.3:c.478-91_478-88del	XP_005250490.1:n.478-91_478-88del
XR_242246.3:n.2323-91_2323-88del
XM_017012319.2:c.478-91_478-88del	XP_016867808.1:n.478-91_478-88del
XR_001744808.2:n.1254-91_1254-88del
XR_242246.5:n.2274-91_2274-88del
NM_000466.3:c.2227-91_2227-88del MANE Select	NP_000457.1:n.2227-91_2227-88del
NM_001282677.2:c.2056-91_2056-88del	NP_001269606.1:n.2056-91_2056-88del
NM_001282678.2:c.1603-91_1603-88del	NP_001269607.1:n.1603-91_1603-88del