Canonical Allele Identifier: CA365766785

Gene: PEX7

Linked Data

• MyVariant Identifiers: chr6:g.137219356T>A (hg19) ; chr6:g.136898218T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.136898218T>A , CM000668.2:g.136898218T>A	GRCh38
NC_000006.11:g.137219356T>A , CM000668.1:g.137219356T>A	GRCh37
NC_000006.10:g.137261049T>A	NCBI36
NG_008462.1:g.80639T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318471.5:c.880T>A MANE Select	ENSP00000315680.3:p.Phe294Ile
ENST00000541292.6:c.*145T>A	ENSP00000441004.1:n.*145T>A
ENST00000678002.1:c.568T>A
ENST00000678557.1:c.766T>A	ENSP00000502962.1:p.Phe256Ile
ENST00000679286.1:c.760T>A	ENSP00000503168.1:p.Phe254Ile
ENST00000318471.4:c.880T>A	ENSP00000315680.3:p.Phe294Ile
NM_000288.3:c.880T>A	NP_000279.1:p.Phe294Ile
XM_005267019.3:c.766T>A	XP_005267076.1:p.Phe256Ile
XM_006715502.1:c.586T>A	XP_006715565.1:p.Phe196Ile
XM_011535900.1:c.*3T>A	XP_011534202.1:n.*3T>A
XM_005267019.4:c.766T>A	XP_005267076.1:p.Phe256Ile
XM_006715502.2:c.586T>A	XP_006715565.1:p.Phe196Ile
XM_017010934.2:c.*3T>A	XP_016866423.1:n.*3T>A
NM_000288.4:c.880T>A MANE Select	NP_000279.1:p.Phe294Ile