Canonical Allele Identifier: CA365762836

Gene: PEX7

Linked Data

• MyVariant Identifiers: chr6:g.137187785T>A (hg19) ; chr6:g.136866647T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.136866647T>A , CM000668.2:g.136866647T>A	GRCh38
NC_000006.11:g.137187785T>A , CM000668.1:g.137187785T>A	GRCh37
NC_000006.10:g.137229478T>A	NCBI36
NG_008462.1:g.49068T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318471.5:c.547T>A MANE Select	ENSP00000315680.3:p.Trp183Arg
ENST00000541292.6:c.547T>A	ENSP00000441004.1:p.Trp183Arg
ENST00000678002.1:c.235T>A
ENST00000678557.1:c.433T>A	ENSP00000502962.1:p.Trp145Arg
ENST00000678593.1:c.552T>A	ENSP00000503841.1:n.552T>A
ENST00000679286.1:c.427T>A	ENSP00000503168.1:p.Trp143Arg
ENST00000318471.4:c.547T>A	ENSP00000315680.3:p.Trp183Arg
ENST00000541292.5:c.547T>A	ENSP00000441004.1:p.Trp183Arg
NM_000288.3:c.547T>A	NP_000279.1:p.Trp183Arg
XM_005267019.3:c.433T>A	XP_005267076.1:p.Trp145Arg
XM_006715502.1:c.340-3243T>A	XP_006715565.1:n.340-3243T>A
XM_011535900.1:c.526+20466T>A	XP_011534202.1:n.526+20466T>A
XM_005267019.4:c.433T>A	XP_005267076.1:p.Trp145Arg
XM_006715502.2:c.340-3243T>A	XP_006715565.1:n.340-3243T>A
XM_017010934.2:c.526+20466T>A	XP_016866423.1:n.526+20466T>A
NM_000288.4:c.547T>A MANE Select	NP_000279.1:p.Trp183Arg