Canonical Allele Identifier: CA365766701

Gene: PEX7

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000318471.5:c.859G>C MANE Select	ENSP00000315680.3:p.Glu287Gln
ENST00000541292.6:c.*124G>C	ENSP00000441004.1:n.*124G>C
ENST00000678002.1:c.547G>C
ENST00000678557.1:c.745G>C	ENSP00000502962.1:p.Glu249Gln
ENST00000679286.1:c.739G>C	ENSP00000503168.1:p.Glu247Gln
ENST00000318471.4:c.859G>C	ENSP00000315680.3:p.Glu287Gln
NM_000288.3:c.859G>C	NP_000279.1:p.Glu287Gln
XM_005267019.3:c.745G>C	XP_005267076.1:p.Glu249Gln
XM_006715502.1:c.565G>C	XP_006715565.1:p.Glu189Gln
XM_011535900.1:c.582G>C	XP_011534202.1:p.Gln194His
XM_005267019.4:c.745G>C	XP_005267076.1:p.Glu249Gln
XM_006715502.2:c.565G>C	XP_006715565.1:p.Glu189Gln
XM_017010934.2:c.582G>C	XP_016866423.1:p.Gln194His
NM_000288.4:c.859G>C MANE Select	NP_000279.1:p.Glu287Gln