Canonical Allele Identifier: CA365764485

Gene: PEX7

Linked Data

• MyVariant Identifiers: chr6:g.137193384A>G (hg19) ; chr6:g.136872246A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.136872246A>G , CM000668.2:g.136872246A>G	GRCh38
NC_000006.11:g.137193384A>G , CM000668.1:g.137193384A>G	GRCh37
NC_000006.10:g.137235077A>G	NCBI36
NG_008462.1:g.54667A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318471.5:c.796A>G MANE Select	ENSP00000315680.3:p.Thr266Ala
ENST00000541292.6:c.*61A>G	ENSP00000441004.1:n.*61A>G
ENST00000678002.1:c.484A>G
ENST00000678557.1:c.682A>G	ENSP00000502962.1:p.Thr228Ala
ENST00000678593.1:c.801A>G	ENSP00000503841.1:n.801A>G
ENST00000679286.1:c.676A>G	ENSP00000503168.1:p.Thr226Ala
ENST00000318471.4:c.796A>G	ENSP00000315680.3:p.Thr266Ala
NM_000288.3:c.796A>G	NP_000279.1:p.Thr266Ala
XM_005267019.3:c.682A>G	XP_005267076.1:p.Thr228Ala
XM_006715502.1:c.502A>G	XP_006715565.1:p.Thr168Ala
XM_011535900.1:c.527-25896A>G	XP_011534202.1:n.527-25896A>G
XM_005267019.4:c.682A>G	XP_005267076.1:p.Thr228Ala
XM_006715502.2:c.502A>G	XP_006715565.1:p.Thr168Ala
XM_017010934.2:c.527-25896A>G	XP_016866423.1:n.527-25896A>G
NM_000288.4:c.796A>G MANE Select	NP_000279.1:p.Thr266Ala