Canonical Allele Identifier: CA365856008
Gene: PEX7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.136826455G>T , CM000668.2:g.136826455G>T GRCh38
NC_000006.11:g.137147593G>T , CM000668.1:g.137147593G>T GRCh37
NC_000006.10:g.137189286G>T NCBI36
NG_008462.1:g.8876G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000318471.5:c.325G>T MANE Select ENSP00000315680.3:p.Glu109Ter
ENST00000541292.6:c.325G>T ENSP00000441004.1:p.Glu109Ter
ENST00000678002.1:c.200G>T
ENST00000678557.1:c.211G>T ENSP00000502962.1:p.Glu71Ter
ENST00000678593.1:c.330G>T ENSP00000503841.1:n.330G>T
ENST00000679286.1:c.205G>T ENSP00000503168.1:p.Glu69Ter
ENST00000318471.4:c.325G>T ENSP00000315680.3:p.Glu109Ter
ENST00000367756.8:c.325G>T ENSP00000356730.4:p.Glu109Ter
ENST00000541292.5:c.325G>T ENSP00000441004.1:p.Glu109Ter
NM_000288.3:c.325G>T NP_000279.1:p.Glu109Ter
XM_005267019.3:c.211G>T XP_005267076.1:p.Glu71Ter
XM_006715502.1:c.325G>T XP_006715565.1:p.Glu109Ter
XM_011535900.1:c.325G>T XP_011534202.1:p.Glu109Ter
XM_005267019.4:c.211G>T XP_005267076.1:p.Glu71Ter
XM_006715502.2:c.325G>T XP_006715565.1:p.Glu109Ter
XM_017010934.2:c.325G>T XP_016866423.1:p.Glu109Ter
NM_000288.4:c.325G>T MANE Select NP_000279.1:p.Glu109Ter