Canonical Allele Identifier: CA365766782

Gene: PEX7

Linked Data

• MyVariant Identifiers: chr6:g.137219355C>G (hg19) ; chr6:g.136898217C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.136898217C>G , CM000668.2:g.136898217C>G	GRCh38
NC_000006.11:g.137219355C>G , CM000668.1:g.137219355C>G	GRCh37
NC_000006.10:g.137261048C>G	NCBI36
NG_008462.1:g.80638C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318471.5:c.879C>G MANE Select	ENSP00000315680.3:p.Asp293Glu
ENST00000541292.6:c.*144C>G	ENSP00000441004.1:n.*144C>G
ENST00000678002.1:c.567C>G
ENST00000678557.1:c.765C>G	ENSP00000502962.1:p.Asp255Glu
ENST00000679286.1:c.759C>G	ENSP00000503168.1:p.Asp253Glu
ENST00000318471.4:c.879C>G	ENSP00000315680.3:p.Asp293Glu
NM_000288.3:c.879C>G	NP_000279.1:p.Asp293Glu
XM_005267019.3:c.765C>G	XP_005267076.1:p.Asp255Glu
XM_006715502.1:c.585C>G	XP_006715565.1:p.Asp195Glu
XM_011535900.1:c.*2C>G	XP_011534202.1:n.*2C>G
XM_005267019.4:c.765C>G	XP_005267076.1:p.Asp255Glu
XM_006715502.2:c.585C>G	XP_006715565.1:p.Asp195Glu
XM_017010934.2:c.*2C>G	XP_016866423.1:n.*2C>G
NM_000288.4:c.879C>G MANE Select	NP_000279.1:p.Asp293Glu