Canonical Allele Identifier: CA365855808

Gene: PEX7

Linked Data

• MyVariant Identifiers: chr6:g.137147499G>C (hg19) ; chr6:g.136826361G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.136826361G>C , CM000668.2:g.136826361G>C	GRCh38
NC_000006.11:g.137147499G>C , CM000668.1:g.137147499G>C	GRCh37
NC_000006.10:g.137189192G>C	NCBI36
NG_008462.1:g.8782G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318471.5:c.231G>C MANE Select	ENSP00000315680.3:p.Glu77Asp
ENST00000541292.6:c.231G>C	ENSP00000441004.1:p.Glu77Asp
ENST00000678002.1:c.106G>C
ENST00000678557.1:c.117G>C	ENSP00000502962.1:p.Glu39Asp
ENST00000678593.1:c.236G>C	ENSP00000503841.1:n.236G>C
ENST00000679286.1:c.111G>C	ENSP00000503168.1:p.Glu37Asp
ENST00000318471.4:c.231G>C	ENSP00000315680.3:p.Glu77Asp
ENST00000367756.8:c.231G>C	ENSP00000356730.4:p.Glu77Asp
ENST00000541292.5:c.231G>C	ENSP00000441004.1:p.Glu77Asp
NM_000288.3:c.231G>C	NP_000279.1:p.Glu77Asp
XM_005267019.3:c.117G>C	XP_005267076.1:p.Glu39Asp
XM_006715502.1:c.231G>C	XP_006715565.1:p.Glu77Asp
XM_011535900.1:c.231G>C	XP_011534202.1:p.Glu77Asp
XM_005267019.4:c.117G>C	XP_005267076.1:p.Glu39Asp
XM_006715502.2:c.231G>C	XP_006715565.1:p.Glu77Asp
XM_017010934.2:c.231G>C	XP_016866423.1:p.Glu77Asp
NM_000288.4:c.231G>C MANE Select	NP_000279.1:p.Glu77Asp