Canonical Allele Identifier: CA2773214777

Gene: PEX7

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.136872410_136872411insA , CM000668.2:g.136872410_136872411insA	GRCh38
NC_000006.11:g.137193548_137193549insA , CM000668.1:g.137193548_137193549insA	GRCh37
NC_000006.10:g.137235241_137235242insA	NCBI36
NG_008462.1:g.54831_54832insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318471.5:c.803+157_803+158insA MANE Select	ENSP00000315680.3:n.803+157_803+158insA
ENST00000541292.6:c.*68+157_*68+158insA	ENSP00000441004.1:n.*68+157_*68+158insA
ENST00000678002.1:c.491+157_491+158insA
ENST00000678557.1:c.689+157_689+158insA	ENSP00000502962.1:n.689+157_689+158insA
ENST00000678593.1:c.965_966insA	ENSP00000503841.1:n.965_966insA
ENST00000679286.1:c.683+157_683+158insA	ENSP00000503168.1:n.683+157_683+158insA
ENST00000318471.4:c.803+157_803+158insA	ENSP00000315680.3:n.803+157_803+158insA
NM_000288.3:c.803+157_803+158insA	NP_000279.1:n.803+157_803+158insA
XM_005267019.3:c.689+157_689+158insA	XP_005267076.1:n.689+157_689+158insA
XM_006715502.1:c.509+157_509+158insA	XP_006715565.1:n.509+157_509+158insA
XM_011535900.1:c.527-25732_527-25731insA	XP_011534202.1:n.527-25732_527-25731insA
XM_005267019.4:c.689+157_689+158insA	XP_005267076.1:n.689+157_689+158insA
XM_006715502.2:c.509+157_509+158insA	XP_006715565.1:n.509+157_509+158insA
XM_017010934.2:c.527-25732_527-25731insA	XP_016866423.1:n.527-25732_527-25731insA
NM_000288.4:c.803+157_803+158insA MANE Select	NP_000279.1:n.803+157_803+158insA