Canonical Allele Identifier: CA2680490155

Gene: PEX7

Linked Data

• gnomAD v4: 6-136898067-ATATCTATT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.136898069_136898076del , CM000668.2:g.136898069_136898076del	GRCh38
NC_000006.11:g.137219207_137219214del , CM000668.1:g.137219207_137219214del	GRCh37
NC_000006.10:g.137260900_137260907del	NCBI36
NG_008462.1:g.80490_80497del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318471.5:c.804-73_804-66del MANE Select	ENSP00000315680.3:n.804-73_804-66del
ENST00000541292.6:c.*69-73_*69-66del	ENSP00000441004.1:n.*69-73_*69-66del
ENST00000678002.1:c.492-73_492-66del
ENST00000678557.1:c.690-73_690-66del	ENSP00000502962.1:n.690-73_690-66del
ENST00000679286.1:c.684-73_684-66del	ENSP00000503168.1:n.684-73_684-66del
ENST00000318471.4:c.804-73_804-66del	ENSP00000315680.3:n.804-73_804-66del
NM_000288.3:c.804-73_804-66del	NP_000279.1:n.804-73_804-66del
XM_005267019.3:c.690-73_690-66del	XP_005267076.1:n.690-73_690-66del
XM_006715502.1:c.510-73_510-66del	XP_006715565.1:n.510-73_510-66del
XM_011535900.1:c.527-73_527-66del	XP_011534202.1:n.527-73_527-66del
XM_005267019.4:c.690-73_690-66del	XP_005267076.1:n.690-73_690-66del
XM_006715502.2:c.510-73_510-66del	XP_006715565.1:n.510-73_510-66del
XM_017010934.2:c.527-73_527-66del	XP_016866423.1:n.527-73_527-66del
NM_000288.4:c.804-73_804-66del MANE Select	NP_000279.1:n.804-73_804-66del