Canonical Allele Identifier: CA365766699

Gene: PEX7

Linked Data

• MyVariant Identifiers: chr6:g.137219335G>A (hg19) ; chr6:g.136898197G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.136898197G>A , CM000668.2:g.136898197G>A	GRCh38
NC_000006.11:g.137219335G>A , CM000668.1:g.137219335G>A	GRCh37
NC_000006.10:g.137261028G>A	NCBI36
NG_008462.1:g.80618G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000318471.5:c.859G>A MANE Select	ENSP00000315680.3:p.Glu287Lys
ENST00000541292.6:c.*124G>A	ENSP00000441004.1:n.*124G>A
ENST00000678002.1:c.547G>A
ENST00000678557.1:c.745G>A	ENSP00000502962.1:p.Glu249Lys
ENST00000679286.1:c.739G>A	ENSP00000503168.1:p.Glu247Lys
ENST00000318471.4:c.859G>A	ENSP00000315680.3:p.Glu287Lys
NM_000288.3:c.859G>A	NP_000279.1:p.Glu287Lys
XM_005267019.3:c.745G>A	XP_005267076.1:p.Glu249Lys
XM_006715502.1:c.565G>A	XP_006715565.1:p.Glu189Lys
XM_011535900.1:c.582G>A	XP_011534202.1:p.Gln194=
XM_005267019.4:c.745G>A	XP_005267076.1:p.Glu249Lys
XM_006715502.2:c.565G>A	XP_006715565.1:p.Glu189Lys
XM_017010934.2:c.582G>A	XP_016866423.1:p.Gln194=
NM_000288.4:c.859G>A MANE Select	NP_000279.1:p.Glu287Lys