Canonical Allele Identifier: CA2773213269

Gene: PEX7

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.136826524_136826527del , CM000668.2:g.136826524_136826527del	GRCh38
NC_000006.11:g.137147662_137147665del , CM000668.1:g.137147662_137147665del	GRCh37
NC_000006.10:g.137189355_137189358del	NCBI36
NG_008462.1:g.8945_8948del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318471.5:c.339+55_339+58del MANE Select	ENSP00000315680.3:n.339+55_339+58del
ENST00000541292.6:c.339+55_339+58del	ENSP00000441004.1:n.339+55_339+58del
ENST00000678002.1:c.214+55_214+58del
ENST00000678557.1:c.225+55_225+58del	ENSP00000502962.1:n.225+55_225+58del
ENST00000678593.1:c.344+55_344+58del	ENSP00000503841.1:n.344+55_344+58del
ENST00000679286.1:c.219+55_219+58del	ENSP00000503168.1:n.219+55_219+58del
ENST00000318471.4:c.339+55_339+58del	ENSP00000315680.3:n.339+55_339+58del
ENST00000367756.8:c.339+55_339+58del	ENSP00000356730.4:n.339+55_339+58del
ENST00000541292.5:c.339+55_339+58del	ENSP00000441004.1:n.339+55_339+58del
NM_000288.3:c.339+55_339+58del	NP_000279.1:n.339+55_339+58del
XM_005267019.3:c.225+55_225+58del	XP_005267076.1:n.225+55_225+58del
XM_006715502.1:c.339+55_339+58del	XP_006715565.1:n.339+55_339+58del
XM_011535900.1:c.339+55_339+58del	XP_011534202.1:n.339+55_339+58del
XM_005267019.4:c.225+55_225+58del	XP_005267076.1:n.225+55_225+58del
XM_006715502.2:c.339+55_339+58del	XP_006715565.1:n.339+55_339+58del
XM_017010934.2:c.339+55_339+58del	XP_016866423.1:n.339+55_339+58del
NM_000288.4:c.339+55_339+58del MANE Select	NP_000279.1:n.339+55_339+58del