Canonical Allele Identifier: CA365764145

Gene: PEX7

Linked Data

• MyVariant Identifiers: chr6:g.137191134G>C (hg19) ; chr6:g.136869996G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.136869996G>C , CM000668.2:g.136869996G>C	GRCh38
NC_000006.11:g.137191134G>C , CM000668.1:g.137191134G>C	GRCh37
NC_000006.10:g.137232827G>C	NCBI36
NG_008462.1:g.52417G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000318471.5:c.740G>C MANE Select	ENSP00000315680.3:p.Arg247Thr
ENST00000541292.6:c.740G>C	ENSP00000441004.1:p.Arg247Thr
ENST00000678002.1:c.428G>C
ENST00000678557.1:c.626G>C	ENSP00000502962.1:p.Arg209Thr
ENST00000678593.1:c.745G>C	ENSP00000503841.1:n.745G>C
ENST00000679286.1:c.620G>C	ENSP00000503168.1:p.Arg207Thr
ENST00000318471.4:c.740G>C	ENSP00000315680.3:p.Arg247Thr
ENST00000541292.5:c.740G>C	ENSP00000441004.1:p.Arg247Thr
NM_000288.3:c.740G>C	NP_000279.1:p.Arg247Thr
XM_005267019.3:c.626G>C	XP_005267076.1:p.Arg209Thr
XM_006715502.1:c.446G>C	XP_006715565.1:p.Arg149Thr
XM_011535900.1:c.526+23815G>C	XP_011534202.1:n.526+23815G>C
XM_005267019.4:c.626G>C	XP_005267076.1:p.Arg209Thr
XM_006715502.2:c.446G>C	XP_006715565.1:p.Arg149Thr
XM_017010934.2:c.526+23815G>C	XP_016866423.1:n.526+23815G>C
NM_000288.4:c.740G>C MANE Select	NP_000279.1:p.Arg247Thr