Canonical Allele Identifier: CA161968969

Gene: PEX1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92511652G>A , CM000669.2:g.92511652G>A	GRCh38
NC_000007.13:g.92140966G>A , CM000669.1:g.92140966G>A	GRCh37
NC_000007.12:g.91978902G>A	NCBI36
NG_008341.1:g.21880C>T
NG_008341.2:g.21880C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000466.3:c.1411C>T MANE Select	NP_000457.1:p.Gln471Ter
ENST00000248633.9:c.1411C>T MANE Select	ENSP00000248633.4:p.Gln471Ter
NM_000466.2:c.1411C>T	NP_000457.1:p.Gln471Ter
NM_001282677.1:c.1411C>T	NP_001269606.1:p.Gln471Ter
NM_001282677.2:c.1411C>T	NP_001269606.1:p.Gln471Ter
NM_001282678.1:c.787C>T	NP_001269607.1:p.Gln263Ter
NM_001282678.2:c.787C>T	NP_001269607.1:p.Gln263Ter
ENST00000248633.8:c.1411C>T	ENSP00000248633.4:p.Gln471Ter
ENST00000422866.1:c.312C>T
ENST00000428214.5:c.1411C>T	ENSP00000394413.1:p.Gln471Ter
ENST00000438045.5:c.445C>T	ENSP00000410438.1:p.Gln149Ter
ENST00000476923.1:n.172C>T
ENST00000484913.5:n.1450C>T
XM_005250433.3:c.-256C>T	XP_005250490.1:n.-256C>T
XM_017012319.2:c.-256C>T	XP_016867808.1:n.-256C>T
XR_001744808.2:n.521C>T
XR_242246.3:n.1507C>T
XR_242246.5:n.1458C>T