Canonical Allele Identifier: CA2683718056

Gene: PEX1

Linked Data

• gnomAD v4: 7-92496586-CTTA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92496590_92496592del , CM000669.2:g.92496590_92496592del	GRCh38
NC_000007.13:g.92125904_92125906del , CM000669.1:g.92125904_92125906del	GRCh37
NC_000007.12:g.91963840_91963842del	NCBI36
NG_008341.1:g.36943_36945del
NG_008341.2:g.36943_36945del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.2783+124_2783+126del MANE Select	ENSP00000248633.4:n.2783+124_2783+126del
ENST00000248633.8:c.2783+124_2783+126del	ENSP00000248633.4:n.2783+124_2783+126del
ENST00000428214.5:c.2612+124_2612+126del	ENSP00000394413.1:n.2612+124_2612+126del
ENST00000438045.5:c.1817+124_1817+126del	ENSP00000410438.1:n.1817+124_1817+126del
ENST00000484913.5:n.2822+124_2822+126del
ENST00000496420.5:n.2675+124_2675+126del
NM_000466.2:c.2783+124_2783+126del	NP_000457.1:n.2783+124_2783+126del
NM_001282677.1:c.2612+124_2612+126del	NP_001269606.1:n.2612+124_2612+126del
NM_001282678.1:c.2159+124_2159+126del	NP_001269607.1:n.2159+124_2159+126del
XM_005250433.3:c.1034+124_1034+126del	XP_005250490.1:n.1034+124_1034+126del
XR_242246.3:n.2879+124_2879+126del
XM_017012319.2:c.1034+124_1034+126del	XP_016867808.1:n.1034+124_1034+126del
XR_001744808.2:n.1810+124_1810+126del
XR_242246.5:n.2830+124_2830+126del
NM_000466.3:c.2783+124_2783+126del MANE Select	NP_000457.1:n.2783+124_2783+126del
NM_001282677.2:c.2612+124_2612+126del	NP_001269606.1:n.2612+124_2612+126del
NM_001282678.2:c.2159+124_2159+126del	NP_001269607.1:n.2159+124_2159+126del