Canonical Allele Identifier: CA365855870
Gene: PEX7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.136826390G>A , CM000668.2:g.136826390G>A GRCh38
NC_000006.11:g.137147528G>A , CM000668.1:g.137147528G>A GRCh37
NC_000006.10:g.137189221G>A NCBI36
NG_008462.1:g.8811G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000318471.5:c.260G>A MANE Select ENSP00000315680.3:p.Ser87Asn
ENST00000541292.6:c.260G>A ENSP00000441004.1:p.Ser87Asn
ENST00000678002.1:c.135G>A
ENST00000678557.1:c.146G>A ENSP00000502962.1:p.Ser49Asn
ENST00000678593.1:c.265G>A ENSP00000503841.1:n.265G>A
ENST00000679286.1:c.140G>A ENSP00000503168.1:p.Ser47Asn
ENST00000318471.4:c.260G>A ENSP00000315680.3:p.Ser87Asn
ENST00000367756.8:c.260G>A ENSP00000356730.4:p.Ser87Asn
ENST00000541292.5:c.260G>A ENSP00000441004.1:p.Ser87Asn
NM_000288.3:c.260G>A NP_000279.1:p.Ser87Asn
XM_005267019.3:c.146G>A XP_005267076.1:p.Ser49Asn
XM_006715502.1:c.260G>A XP_006715565.1:p.Ser87Asn
XM_011535900.1:c.260G>A XP_011534202.1:p.Ser87Asn
XM_005267019.4:c.146G>A XP_005267076.1:p.Ser49Asn
XM_006715502.2:c.260G>A XP_006715565.1:p.Ser87Asn
XM_017010934.2:c.260G>A XP_016866423.1:p.Ser87Asn
NM_000288.4:c.260G>A MANE Select NP_000279.1:p.Ser87Asn