Canonical Allele Identifier: CA365766565

Gene: PEX7

Linked Data

• MyVariant Identifiers: chr6:g.137219297A>G (hg19) ; chr6:g.136898159A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.136898159A>G , CM000668.2:g.136898159A>G	GRCh38
NC_000006.11:g.137219297A>G , CM000668.1:g.137219297A>G	GRCh37
NC_000006.10:g.137260990A>G	NCBI36
NG_008462.1:g.80580A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318471.5:c.821A>G MANE Select	ENSP00000315680.3:p.Lys274Arg
ENST00000541292.6:c.*86A>G	ENSP00000441004.1:n.*86A>G
ENST00000678002.1:c.509A>G
ENST00000678557.1:c.707A>G	ENSP00000502962.1:p.Lys236Arg
ENST00000679286.1:c.701A>G	ENSP00000503168.1:p.Lys234Arg
ENST00000318471.4:c.821A>G	ENSP00000315680.3:p.Lys274Arg
NM_000288.3:c.821A>G	NP_000279.1:p.Lys274Arg
XM_005267019.3:c.707A>G	XP_005267076.1:p.Lys236Arg
XM_006715502.1:c.527A>G	XP_006715565.1:p.Lys176Arg
XM_011535900.1:c.544A>G	XP_011534202.1:p.Ser182Gly
XM_005267019.4:c.707A>G	XP_005267076.1:p.Lys236Arg
XM_006715502.2:c.527A>G	XP_006715565.1:p.Lys176Arg
XM_017010934.2:c.544A>G	XP_016866423.1:p.Ser182Gly
NM_000288.4:c.821A>G MANE Select	NP_000279.1:p.Lys274Arg