Canonical Allele Identifier: CA365766793

Gene: PEX7

Linked Data

• MyVariant Identifiers: chr6:g.137219357T>G (hg19) ; chr6:g.136898219T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.136898219T>G , CM000668.2:g.136898219T>G	GRCh38
NC_000006.11:g.137219357T>G , CM000668.1:g.137219357T>G	GRCh37
NC_000006.10:g.137261050T>G	NCBI36
NG_008462.1:g.80640T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318471.5:c.881T>G MANE Select	ENSP00000315680.3:p.Phe294Cys
ENST00000541292.6:c.*146T>G	ENSP00000441004.1:n.*146T>G
ENST00000678002.1:c.569T>G
ENST00000678557.1:c.767T>G	ENSP00000502962.1:p.Phe256Cys
ENST00000679286.1:c.761T>G	ENSP00000503168.1:p.Phe254Cys
ENST00000318471.4:c.881T>G	ENSP00000315680.3:p.Phe294Cys
NM_000288.3:c.881T>G	NP_000279.1:p.Phe294Cys
XM_005267019.3:c.767T>G	XP_005267076.1:p.Phe256Cys
XM_006715502.1:c.587T>G	XP_006715565.1:p.Phe196Cys
XM_011535900.1:c.*4T>G	XP_011534202.1:n.*4T>G
XM_005267019.4:c.767T>G	XP_005267076.1:p.Phe256Cys
XM_006715502.2:c.587T>G	XP_006715565.1:p.Phe196Cys
XM_017010934.2:c.*4T>G	XP_016866423.1:n.*4T>G
NM_000288.4:c.881T>G MANE Select	NP_000279.1:p.Phe294Cys