Canonical Allele Identifier: CA368170977

Gene: PEX1

Linked Data

• MyVariant Identifiers: chr7:g.92126052G>A (hg19) ; chr7:g.92496738G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92496738G>A , CM000669.2:g.92496738G>A	GRCh38
NC_000007.13:g.92126052G>A , CM000669.1:g.92126052G>A	GRCh37
NC_000007.12:g.91963988G>A	NCBI36
NG_008341.1:g.36794C>T
NG_008341.2:g.36794C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.2758C>T MANE Select	ENSP00000248633.4:p.Gln920Ter
ENST00000248633.8:c.2758C>T	ENSP00000248633.4:p.Gln920Ter
ENST00000428214.5:c.2587C>T	ENSP00000394413.1:p.Gln863Ter
ENST00000438045.5:c.1792C>T	ENSP00000410438.1:p.Gln598Ter
ENST00000484913.5:n.2797C>T
ENST00000496420.5:n.2650C>T
NM_000466.2:c.2758C>T	NP_000457.1:p.Gln920Ter
NM_001282677.1:c.2587C>T	NP_001269606.1:p.Gln863Ter
NM_001282678.1:c.2134C>T	NP_001269607.1:p.Gln712Ter
XM_005250433.3:c.1009C>T	XP_005250490.1:p.Gln337Ter
XR_242246.3:n.2854C>T
XM_017012319.2:c.1009C>T	XP_016867808.1:p.Gln337Ter
XR_001744808.2:n.1785C>T
XR_242246.5:n.2805C>T
NM_000466.3:c.2758C>T MANE Select	NP_000457.1:p.Gln920Ter
NM_001282677.2:c.2587C>T	NP_001269606.1:p.Gln863Ter
NM_001282678.2:c.2134C>T	NP_001269607.1:p.Gln712Ter