Canonical Allele Identifier: CA365855855
Gene: PEX7 HGNC NCBI

Linked Data

dbSNP Id: rs745706327

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.136826383A>T , CM000668.2:g.136826383A>T GRCh38
NC_000006.11:g.137147521A>T , CM000668.1:g.137147521A>T GRCh37
NC_000006.10:g.137189214A>T NCBI36
NG_008462.1:g.8804A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000318471.5:c.253A>T MANE Select ENSP00000315680.3:p.Thr85Ser
ENST00000541292.6:c.253A>T ENSP00000441004.1:p.Thr85Ser
ENST00000678002.1:c.128A>T
ENST00000678557.1:c.139A>T ENSP00000502962.1:p.Thr47Ser
ENST00000678593.1:c.258A>T ENSP00000503841.1:n.258A>T
ENST00000679286.1:c.133A>T ENSP00000503168.1:p.Thr45Ser
ENST00000318471.4:c.253A>T ENSP00000315680.3:p.Thr85Ser
ENST00000367756.8:c.253A>T ENSP00000356730.4:p.Thr85Ser
ENST00000541292.5:c.253A>T ENSP00000441004.1:p.Thr85Ser
NM_000288.3:c.253A>T NP_000279.1:p.Thr85Ser
XM_005267019.3:c.139A>T XP_005267076.1:p.Thr47Ser
XM_006715502.1:c.253A>T XP_006715565.1:p.Thr85Ser
XM_011535900.1:c.253A>T XP_011534202.1:p.Thr85Ser
XM_005267019.4:c.139A>T XP_005267076.1:p.Thr47Ser
XM_006715502.2:c.253A>T XP_006715565.1:p.Thr85Ser
XM_017010934.2:c.253A>T XP_016866423.1:p.Thr85Ser
NM_000288.4:c.253A>T MANE Select NP_000279.1:p.Thr85Ser