Canonical Allele Identifier: CA119074

Gene: PEX7

Linked Data

• ClinVar Variation Id: 7787
• ClinVar RCV Id: RCV000008229 ; RCV000032116 ; RCV000393497 ; RCV000731239
• dbSNP Id: rs267608255
• ExAC: 6:137166743 A / G
• gnomAD v2: 6-137166743-A-G
• gnomAD v3: 6-136845605-A-G
• gnomAD v4: 6-136845605-A-G
• MyVariant Identifiers: chr6:g.137166743A>G (hg19) ; chr6:g.136845605A>G (hg38)
• PubMed: PMID:12325024 ; PMID:20301447

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.136845605A>G , CM000668.2:g.136845605A>G	GRCh38
NC_000006.11:g.137166743A>G , CM000668.1:g.137166743A>G	GRCh37
NC_000006.10:g.137208436A>G	NCBI36
NG_008462.1:g.28026A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318471.5:c.340-10A>G MANE Select	ENSP00000315680.3:n.340-10A>G
ENST00000541292.6:c.340-10A>G	ENSP00000441004.1:n.340-10A>G
ENST00000678002.1:c.214+19136A>G
ENST00000678557.1:c.226-10A>G	ENSP00000502962.1:n.226-10A>G
ENST00000678593.1:c.345-10A>G	ENSP00000503841.1:n.345-10A>G
ENST00000679286.1:c.220-10A>G	ENSP00000503168.1:n.220-10A>G
ENST00000318471.4:c.340-10A>G	ENSP00000315680.3:n.340-10A>G
ENST00000541292.5:c.340-10A>G	ENSP00000441004.1:n.340-10A>G
NM_000288.3:c.340-10A>G	NP_000279.1:n.340-10A>G
XM_005267019.3:c.226-10A>G	XP_005267076.1:n.226-10A>G
XM_006715502.1:c.339+19136A>G	XP_006715565.1:n.339+19136A>G
XM_011535900.1:c.340-10A>G	XP_011534202.1:n.340-10A>G
XM_005267019.4:c.226-10A>G	XP_005267076.1:n.226-10A>G
XM_006715502.2:c.339+19136A>G	XP_006715565.1:n.339+19136A>G
XM_017010934.2:c.340-10A>G	XP_016866423.1:n.340-10A>G
NM_000288.4:c.340-10A>G MANE Select	NP_000279.1:n.340-10A>G