Canonical Allele Identifier: CA365766766

Gene: PEX7

Linked Data

• MyVariant Identifiers: chr6:g.137219351T>G (hg19) ; chr6:g.136898213T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.136898213T>G , CM000668.2:g.136898213T>G	GRCh38
NC_000006.11:g.137219351T>G , CM000668.1:g.137219351T>G	GRCh37
NC_000006.10:g.137261044T>G	NCBI36
NG_008462.1:g.80634T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318471.5:c.875T>G MANE Select	ENSP00000315680.3:p.Leu292Ter
ENST00000541292.6:c.*140T>G	ENSP00000441004.1:n.*140T>G
ENST00000678002.1:c.563T>G
ENST00000678557.1:c.761T>G	ENSP00000502962.1:p.Leu254Ter
ENST00000679286.1:c.755T>G	ENSP00000503168.1:p.Leu252Ter
ENST00000318471.4:c.875T>G	ENSP00000315680.3:p.Leu292Ter
NM_000288.3:c.875T>G	NP_000279.1:p.Leu292Ter
XM_005267019.3:c.761T>G	XP_005267076.1:p.Leu254Ter
XM_006715502.1:c.581T>G	XP_006715565.1:p.Leu194Ter
XM_011535900.1:c.598T>G	XP_011534202.1:p.Ter200Glu
XM_005267019.4:c.761T>G	XP_005267076.1:p.Leu254Ter
XM_006715502.2:c.581T>G	XP_006715565.1:p.Leu194Ter
XM_017010934.2:c.598T>G	XP_016866423.1:p.Ter200Glu
NM_000288.4:c.875T>G MANE Select	NP_000279.1:p.Leu292Ter