Canonical Allele Identifier: CA365855814

Gene: PEX7

Linked Data

• MyVariant Identifiers: chr6:g.137147501A>T (hg19) ; chr6:g.136826363A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.136826363A>T , CM000668.2:g.136826363A>T	GRCh38
NC_000006.11:g.137147501A>T , CM000668.1:g.137147501A>T	GRCh37
NC_000006.10:g.137189194A>T	NCBI36
NG_008462.1:g.8784A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318471.5:c.233A>T MANE Select	ENSP00000315680.3:p.Asn78Ile
ENST00000541292.6:c.233A>T	ENSP00000441004.1:p.Asn78Ile
ENST00000678002.1:c.108A>T
ENST00000678557.1:c.119A>T	ENSP00000502962.1:p.Asn40Ile
ENST00000678593.1:c.238A>T	ENSP00000503841.1:n.238A>T
ENST00000679286.1:c.113A>T	ENSP00000503168.1:p.Asn38Ile
ENST00000318471.4:c.233A>T	ENSP00000315680.3:p.Asn78Ile
ENST00000367756.8:c.233A>T	ENSP00000356730.4:p.Asn78Ile
ENST00000541292.5:c.233A>T	ENSP00000441004.1:p.Asn78Ile
NM_000288.3:c.233A>T	NP_000279.1:p.Asn78Ile
XM_005267019.3:c.119A>T	XP_005267076.1:p.Asn40Ile
XM_006715502.1:c.233A>T	XP_006715565.1:p.Asn78Ile
XM_011535900.1:c.233A>T	XP_011534202.1:p.Asn78Ile
XM_005267019.4:c.119A>T	XP_005267076.1:p.Asn40Ile
XM_006715502.2:c.233A>T	XP_006715565.1:p.Asn78Ile
XM_017010934.2:c.233A>T	XP_016866423.1:p.Asn78Ile
NM_000288.4:c.233A>T MANE Select	NP_000279.1:p.Asn78Ile