Canonical Allele Identifier: CA1094888308

Gene: PEX7

Linked Data

• dbSNP Id: rs1774184616
• gnomAD v3: 6-136826106-C-CCA
• gnomAD v4: 6-136826106-C-CCA

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.136826106_136826107insCA , CM000668.2:g.136826106_136826107insCA	GRCh38
NC_000006.11:g.137147244_137147245insCA , CM000668.1:g.137147244_137147245insCA	GRCh37
NC_000006.10:g.137188937_137188938insCA	NCBI36
NG_008462.1:g.8527_8528insCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318471.5:c.189-213_189-212insCA MANE Select	ENSP00000315680.3:n.189-213_189-212insCA
ENST00000541292.6:c.189-213_189-212insCA	ENSP00000441004.1:n.189-213_189-212insCA
ENST00000678002.1:c.59-208_59-207insCA
ENST00000678557.1:c.75-213_75-212insCA	ENSP00000502962.1:n.75-213_75-212insCA
ENST00000678593.1:c.189-208_189-207insCA	ENSP00000503841.1:n.189-208_189-207insCA
ENST00000679286.1:c.69-213_69-212insCA	ENSP00000503168.1:n.69-213_69-212insCA
ENST00000318471.4:c.189-213_189-212insCA	ENSP00000315680.3:n.189-213_189-212insCA
ENST00000367756.8:c.189-213_189-212insCA	ENSP00000356730.4:n.189-213_189-212insCA
ENST00000541292.5:c.189-213_189-212insCA	ENSP00000441004.1:n.189-213_189-212insCA
NM_000288.3:c.189-213_189-212insCA	NP_000279.1:n.189-213_189-212insCA
XM_005267019.3:c.75-213_75-212insCA	XP_005267076.1:n.75-213_75-212insCA
XM_006715502.1:c.189-213_189-212insCA	XP_006715565.1:n.189-213_189-212insCA
XM_011535900.1:c.189-213_189-212insCA	XP_011534202.1:n.189-213_189-212insCA
XM_005267019.4:c.75-213_75-212insCA	XP_005267076.1:n.75-213_75-212insCA
XM_006715502.2:c.189-213_189-212insCA	XP_006715565.1:n.189-213_189-212insCA
XM_017010934.2:c.189-213_189-212insCA	XP_016866423.1:n.189-213_189-212insCA
NM_000288.4:c.189-213_189-212insCA MANE Select	NP_000279.1:n.189-213_189-212insCA