Canonical Allele Identifier: CA365855888
Gene: PEX7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.136826398G>A , CM000668.2:g.136826398G>A GRCh38
NC_000006.11:g.137147536G>A , CM000668.1:g.137147536G>A GRCh37
NC_000006.10:g.137189229G>A NCBI36
NG_008462.1:g.8819G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000318471.5:c.268G>A MANE Select ENSP00000315680.3:p.Gly90Ser
ENST00000541292.6:c.268G>A ENSP00000441004.1:p.Gly90Ser
ENST00000678002.1:c.143G>A
ENST00000678557.1:c.154G>A ENSP00000502962.1:p.Gly52Ser
ENST00000678593.1:c.273G>A ENSP00000503841.1:n.273G>A
ENST00000679286.1:c.148G>A ENSP00000503168.1:p.Gly50Ser
ENST00000318471.4:c.268G>A ENSP00000315680.3:p.Gly90Ser
ENST00000367756.8:c.268G>A ENSP00000356730.4:p.Gly90Ser
ENST00000541292.5:c.268G>A ENSP00000441004.1:p.Gly90Ser
NM_000288.3:c.268G>A NP_000279.1:p.Gly90Ser
XM_005267019.3:c.154G>A XP_005267076.1:p.Gly52Ser
XM_006715502.1:c.268G>A XP_006715565.1:p.Gly90Ser
XM_011535900.1:c.268G>A XP_011534202.1:p.Gly90Ser
XM_005267019.4:c.154G>A XP_005267076.1:p.Gly52Ser
XM_006715502.2:c.268G>A XP_006715565.1:p.Gly90Ser
XM_017010934.2:c.268G>A XP_016866423.1:p.Gly90Ser
NM_000288.4:c.268G>A MANE Select NP_000279.1:p.Gly90Ser