Canonical Allele Identifier: CA365855713

Gene: PEX7

Linked Data

• MyVariant Identifiers: chr6:g.137147459T>A (hg19) ; chr6:g.136826321T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.136826321T>A , CM000668.2:g.136826321T>A	GRCh38
NC_000006.11:g.137147459T>A , CM000668.1:g.137147459T>A	GRCh37
NC_000006.10:g.137189152T>A	NCBI36
NG_008462.1:g.8742T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000318471.5:c.191T>A MANE Select	ENSP00000315680.3:p.Phe64Tyr
ENST00000541292.6:c.191T>A	ENSP00000441004.1:p.Phe64Tyr
ENST00000678002.1:c.66T>A
ENST00000678557.1:c.77T>A	ENSP00000502962.1:p.Phe26Tyr
ENST00000678593.1:c.196T>A	ENSP00000503841.1:p.Leu66Met
ENST00000679286.1:c.71T>A	ENSP00000503168.1:p.Phe24Tyr
ENST00000318471.4:c.191T>A	ENSP00000315680.3:p.Phe64Tyr
ENST00000367756.8:c.191T>A	ENSP00000356730.4:p.Phe64Tyr
ENST00000541292.5:c.191T>A	ENSP00000441004.1:p.Phe64Tyr
NM_000288.3:c.191T>A	NP_000279.1:p.Phe64Tyr
XM_005267019.3:c.77T>A	XP_005267076.1:p.Phe26Tyr
XM_006715502.1:c.191T>A	XP_006715565.1:p.Phe64Tyr
XM_011535900.1:c.191T>A	XP_011534202.1:p.Phe64Tyr
XM_005267019.4:c.77T>A	XP_005267076.1:p.Phe26Tyr
XM_006715502.2:c.191T>A	XP_006715565.1:p.Phe64Tyr
XM_017010934.2:c.191T>A	XP_016866423.1:p.Phe64Tyr
NM_000288.4:c.191T>A MANE Select	NP_000279.1:p.Phe64Tyr