Canonical Allele Identifier: CA2680487839

Gene: PEX7

Linked Data

• gnomAD v4: 6-136822591-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.136822593del , CM000668.2:g.136822593del	GRCh38
NC_000006.11:g.137143731del , CM000668.1:g.137143731del	GRCh37
NC_000006.10:g.137185424del	NCBI36
NG_008462.1:g.5014del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318471.5:c.-73del MANE Select	ENSP00000315680.3:n.-73del
ENST00000541292.6:c.-73del	ENSP00000441004.1:n.-73del
ENST00000318471.4:c.-73del	ENSP00000315680.3:n.-73del
ENST00000367756.8:c.-73del	ENSP00000356730.4:n.-73del
ENST00000541292.5:c.-73del	ENSP00000441004.1:n.-73del
NM_000288.3:c.-73del	NP_000279.1:n.-73del
XM_006715502.1:c.-73del	XP_006715565.1:n.-73del
XM_011535900.1:c.-73del	XP_011534202.1:n.-73del
XM_006715502.2:c.-73del	XP_006715565.1:n.-73del
XM_017010934.2:c.-73del	XP_016866423.1:n.-73del
NM_000288.4:c.-73del MANE Select	NP_000279.1:n.-73del