Canonical Allele Identifier: CA2840505767

Gene: PEX7

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.136872313dup , CM000668.2:g.136872313dup	GRCh38
NC_000006.11:g.137193451dup , CM000668.1:g.137193451dup	GRCh37
NC_000006.10:g.137235144dup	NCBI36
NG_008462.1:g.54734dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318471.5:c.803+60dup MANE Select	ENSP00000315680.3:n.803+60dup
ENST00000541292.6:c.*68+60dup	ENSP00000441004.1:n.*68+60dup
ENST00000678002.1:c.491+60dup
ENST00000678557.1:c.689+60dup	ENSP00000502962.1:n.689+60dup
ENST00000678593.1:c.868dup	ENSP00000503841.1:n.868dup
ENST00000679286.1:c.683+60dup	ENSP00000503168.1:n.683+60dup
ENST00000318471.4:c.803+60dup	ENSP00000315680.3:n.803+60dup
NM_000288.3:c.803+60dup	NP_000279.1:n.803+60dup
XM_005267019.3:c.689+60dup	XP_005267076.1:n.689+60dup
XM_006715502.1:c.509+60dup	XP_006715565.1:n.509+60dup
XM_011535900.1:c.527-25829dup	XP_011534202.1:n.527-25829dup
XM_005267019.4:c.689+60dup	XP_005267076.1:n.689+60dup
XM_006715502.2:c.509+60dup	XP_006715565.1:n.509+60dup
XM_017010934.2:c.527-25829dup	XP_016866423.1:n.527-25829dup
NM_000288.4:c.803+60dup MANE Select	NP_000279.1:n.803+60dup