Canonical Allele Identifier: CA365855887

Gene: PEX7

Linked Data

• MyVariant Identifiers: chr6:g.137147535T>G (hg19) ; chr6:g.136826397T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.136826397T>G , CM000668.2:g.136826397T>G	GRCh38
NC_000006.11:g.137147535T>G , CM000668.1:g.137147535T>G	GRCh37
NC_000006.10:g.137189228T>G	NCBI36
NG_008462.1:g.8818T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000318471.5:c.267T>G MANE Select	ENSP00000315680.3:p.Asp89Glu
ENST00000541292.6:c.267T>G	ENSP00000441004.1:p.Asp89Glu
ENST00000678002.1:c.142T>G
ENST00000678557.1:c.153T>G	ENSP00000502962.1:p.Asp51Glu
ENST00000678593.1:c.272T>G	ENSP00000503841.1:n.272T>G
ENST00000679286.1:c.147T>G	ENSP00000503168.1:p.Asp49Glu
ENST00000318471.4:c.267T>G	ENSP00000315680.3:p.Asp89Glu
ENST00000367756.8:c.267T>G	ENSP00000356730.4:p.Asp89Glu
ENST00000541292.5:c.267T>G	ENSP00000441004.1:p.Asp89Glu
NM_000288.3:c.267T>G	NP_000279.1:p.Asp89Glu
XM_005267019.3:c.153T>G	XP_005267076.1:p.Asp51Glu
XM_006715502.1:c.267T>G	XP_006715565.1:p.Asp89Glu
XM_011535900.1:c.267T>G	XP_011534202.1:p.Asp89Glu
XM_005267019.4:c.153T>G	XP_005267076.1:p.Asp51Glu
XM_006715502.2:c.267T>G	XP_006715565.1:p.Asp89Glu
XM_017010934.2:c.267T>G	XP_016866423.1:p.Asp89Glu
NM_000288.4:c.267T>G MANE Select	NP_000279.1:p.Asp89Glu