Canonical Allele Identifier: CA365766813

Gene: PEX7

Linked Data

• MyVariant Identifiers: chr6:g.137219362C>G (hg19) ; chr6:g.136898224C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.136898224C>G , CM000668.2:g.136898224C>G	GRCh38
NC_000006.11:g.137219362C>G , CM000668.1:g.137219362C>G	GRCh37
NC_000006.10:g.137261055C>G	NCBI36
NG_008462.1:g.80645C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318471.5:c.886C>G MANE Select	ENSP00000315680.3:p.Leu296Val
ENST00000541292.6:c.*151C>G	ENSP00000441004.1:n.*151C>G
ENST00000678002.1:c.574C>G
ENST00000678557.1:c.772C>G	ENSP00000502962.1:p.Leu258Val
ENST00000679286.1:c.766C>G	ENSP00000503168.1:p.Leu256Val
ENST00000318471.4:c.886C>G	ENSP00000315680.3:p.Leu296Val
NM_000288.3:c.886C>G	NP_000279.1:p.Leu296Val
XM_005267019.3:c.772C>G	XP_005267076.1:p.Leu258Val
XM_006715502.1:c.592C>G	XP_006715565.1:p.Leu198Val
XM_005267019.4:c.772C>G	XP_005267076.1:p.Leu258Val
XM_006715502.2:c.592C>G	XP_006715565.1:p.Leu198Val
XM_017010934.2:c.*9C>G	XP_016866423.1:n.*9C>G
NM_000288.4:c.886C>G MANE Select	NP_000279.1:p.Leu296Val