Canonical Allele Identifier: CA365855476

Gene: PEX7

Linked Data

• dbSNP Id: rs1480725330
• gnomAD v3: 6-136822795-G-A
• gnomAD v4: 6-136822795-G-A
• MyVariant Identifiers: chr6:g.137143933G>A (hg19) ; chr6:g.136822795G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.136822795G>A , CM000668.2:g.136822795G>A	GRCh38
NC_000006.11:g.137143933G>A , CM000668.1:g.137143933G>A	GRCh37
NC_000006.10:g.137185626G>A	NCBI36
NG_008462.1:g.5216G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000318471.5:c.130G>A MANE Select	ENSP00000315680.3:p.Gly44Ser
ENST00000541292.6:c.130G>A	ENSP00000441004.1:p.Gly44Ser
ENST00000678593.1:c.130G>A	ENSP00000503841.1:p.Gly44Ser
ENST00000318471.4:c.130G>A	ENSP00000315680.3:p.Gly44Ser
ENST00000367756.8:c.130G>A	ENSP00000356730.4:p.Gly44Ser
ENST00000541292.5:c.130G>A	ENSP00000441004.1:p.Gly44Ser
NM_000288.3:c.130G>A	NP_000279.1:p.Gly44Ser
XM_006715502.1:c.130G>A	XP_006715565.1:p.Gly44Ser
XM_011535900.1:c.130G>A	XP_011534202.1:p.Gly44Ser
XM_006715502.2:c.130G>A	XP_006715565.1:p.Gly44Ser
XM_017010934.2:c.130G>A	XP_016866423.1:p.Gly44Ser
NM_000288.4:c.130G>A MANE Select	NP_000279.1:p.Gly44Ser