Canonical Allele Identifier: CA365855155

Gene: PEX7

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.136822705A>G , CM000668.2:g.136822705A>G	GRCh38
NC_000006.11:g.137143843A>G , CM000668.1:g.137143843A>G	GRCh37
NC_000006.10:g.137185536A>G	NCBI36
NG_008462.1:g.5126A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318471.5:c.40A>G MANE Select	ENSP00000315680.3:p.Thr14Ala
ENST00000541292.6:c.40A>G	ENSP00000441004.1:p.Thr14Ala
ENST00000678593.1:c.40A>G	ENSP00000503841.1:p.Thr14Ala
ENST00000318471.4:c.40A>G	ENSP00000315680.3:p.Thr14Ala
ENST00000367756.8:c.40A>G	ENSP00000356730.4:p.Thr14Ala
ENST00000541292.5:c.40A>G	ENSP00000441004.1:p.Thr14Ala
NM_000288.3:c.40A>G	NP_000279.1:p.Thr14Ala
XM_006715502.1:c.40A>G	XP_006715565.1:p.Thr14Ala
XM_011535900.1:c.40A>G	XP_011534202.1:p.Thr14Ala
XM_006715502.2:c.40A>G	XP_006715565.1:p.Thr14Ala
XM_017010934.2:c.40A>G	XP_016866423.1:p.Thr14Ala
NM_000288.4:c.40A>G MANE Select	NP_000279.1:p.Thr14Ala