Canonical Allele Identifier: CA658796915

Gene: GPNMB

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.23254241del , CM000669.2:g.23254241del	GRCh38
NC_000007.13:g.23293860del , CM000669.1:g.23293860del	GRCh37
NC_000007.12:g.23260385del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_002510.3:c.296del MANE Select	NP_002501.1:p.Asn99ThrfsTer2
ENST00000258733.9:c.296del MANE Select	ENSP00000258733.5:p.Asn99ThrfsTer2
NM_001005340.1:c.296del	NP_001005340.1:p.Asn99ThrfsTer2
NM_001005340.2:c.296del	NP_001005340.1:p.Asn99ThrfsTer2
NM_002510.2:c.296del	NP_002501.1:p.Asn99ThrfsTer2
ENST00000258733.8:c.296del	ENSP00000258733.4:p.Asn99ThrfsTer2
ENST00000381990.6:c.296del	ENSP00000371420.2:p.Asn99ThrfsTer2
ENST00000409458.3:c.296del	ENSP00000386476.3:p.Asn99ThrfsTer2
ENST00000465673.5:n.474del
ENST00000487890.5:n.487del
ENST00000492512.1:n.376del
ENST00000492858.6:n.498del
ENST00000647578.1:c.296del	ENSP00000497362.1:p.Asn99ThrfsTer2
XM_005249578.1:c.296del	XP_005249635.1:p.Asn99ThrfsTer2
XM_005249578.3:c.296del	XP_005249635.1:p.Asn99ThrfsTer2
XM_017011676.2:c.296del	XP_016867165.1:p.Asn99ThrfsTer2
XM_017011677.2:c.296del	XP_016867166.1:p.Asn99ThrfsTer2
XM_017011678.2:c.296del	XP_016867167.1:p.Asn99ThrfsTer2