Canonical Allele Identifier: CA365855753

Gene: PEX7

Linked Data

• MyVariant Identifiers: chr6:g.137147474G>T (hg19) ; chr6:g.136826336G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.136826336G>T , CM000668.2:g.136826336G>T	GRCh38
NC_000006.11:g.137147474G>T , CM000668.1:g.137147474G>T	GRCh37
NC_000006.10:g.137189167G>T	NCBI36
NG_008462.1:g.8757G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318471.5:c.206G>T MANE Select	ENSP00000315680.3:p.Gly69Val
ENST00000541292.6:c.206G>T	ENSP00000441004.1:p.Gly69Val
ENST00000678002.1:c.81G>T
ENST00000678557.1:c.92G>T	ENSP00000502962.1:p.Gly31Val
ENST00000678593.1:c.211G>T	ENSP00000503841.1:p.Val71Phe
ENST00000679286.1:c.86G>T	ENSP00000503168.1:p.Gly29Val
ENST00000318471.4:c.206G>T	ENSP00000315680.3:p.Gly69Val
ENST00000367756.8:c.206G>T	ENSP00000356730.4:p.Gly69Val
ENST00000541292.5:c.206G>T	ENSP00000441004.1:p.Gly69Val
NM_000288.3:c.206G>T	NP_000279.1:p.Gly69Val
XM_005267019.3:c.92G>T	XP_005267076.1:p.Gly31Val
XM_006715502.1:c.206G>T	XP_006715565.1:p.Gly69Val
XM_011535900.1:c.206G>T	XP_011534202.1:p.Gly69Val
XM_005267019.4:c.92G>T	XP_005267076.1:p.Gly31Val
XM_006715502.2:c.206G>T	XP_006715565.1:p.Gly69Val
XM_017010934.2:c.206G>T	XP_016866423.1:p.Gly69Val
NM_000288.4:c.206G>T MANE Select	NP_000279.1:p.Gly69Val