Canonical Allele Identifier: CA452231827

Gene: PEX7

Linked Data

• MyVariant Identifiers: chr6:g.137219376T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.136898238T>G , CM000668.2:g.136898238T>G	GRCh38
NC_000006.11:g.137219376T>G , CM000668.1:g.137219376T>G	GRCh37
NC_000006.10:g.137261069T>G	NCBI36
NG_008462.1:g.80659T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318471.5:c.900T>G MANE Select	ENSP00000315680.3:p.Thr300=
ENST00000541292.6:c.*165T>G	ENSP00000441004.1:n.*165T>G
ENST00000678002.1:c.588T>G
ENST00000678557.1:c.786T>G	ENSP00000502962.1:p.Thr262=
ENST00000679286.1:c.780T>G	ENSP00000503168.1:p.Thr260=
ENST00000318471.4:c.900T>G	ENSP00000315680.3:p.Thr300=
NM_000288.3:c.900T>G	NP_000279.1:p.Thr300=
XM_005267019.3:c.786T>G	XP_005267076.1:p.Thr262=
XM_006715502.1:c.606T>G	XP_006715565.1:p.Thr202=
XM_005267019.4:c.786T>G	XP_005267076.1:p.Thr262=
XM_006715502.2:c.606T>G	XP_006715565.1:p.Thr202=
XM_017010934.2:c.*23T>G	XP_016866423.1:n.*23T>G
NM_000288.4:c.900T>G MANE Select	NP_000279.1:p.Thr300=