Canonical Allele Identifier: CA2682036543

Gene: GPNMB

Linked Data

• gnomAD v4: 7-23254036-CA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.23254040del , CM000669.2:g.23254040del	GRCh38
NC_000007.13:g.23293659del , CM000669.1:g.23293659del	GRCh37
NC_000007.12:g.23260184del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000258733.9:c.224-129del MANE Select	ENSP00000258733.5:n.224-129del
ENST00000647578.1:c.224-129del	ENSP00000497362.1:n.224-129del
ENST00000258733.8:c.224-129del	ENSP00000258733.4:n.224-129del
ENST00000381990.6:c.224-129del	ENSP00000371420.2:n.224-129del
ENST00000409458.3:c.224-129del	ENSP00000386476.3:n.224-129del
ENST00000465673.5:n.402-129del
ENST00000487890.5:n.415-129del
ENST00000492512.1:n.304-129del
ENST00000492858.6:n.426-129del
NM_001005340.1:c.224-129del	NP_001005340.1:n.224-129del
NM_002510.2:c.224-129del	NP_002501.1:n.224-129del
XM_005249578.1:c.224-129del	XP_005249635.1:n.224-129del
XM_005249578.3:c.224-129del	XP_005249635.1:n.224-129del
XM_017011676.2:c.224-129del	XP_016867165.1:n.224-129del
XM_017011677.2:c.224-129del	XP_016867166.1:n.224-129del
XM_017011678.2:c.224-129del	XP_016867167.1:n.224-129del
NM_001005340.2:c.224-129del	NP_001005340.1:n.224-129del
NM_002510.3:c.224-129del MANE Select	NP_002501.1:n.224-129del