Canonical Allele Identifier: CA1694388015

Gene: GPNMB

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.23254027T= , CM000669.2:g.23254027T=	GRCh38
NC_000007.13:g.23293646T= , CM000669.1:g.23293646T=	GRCh37
NC_000007.12:g.23260171T=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000258733.9:c.224-142T= MANE Select	ENSP00000258733.5:n.224-142T=
ENST00000647578.1:c.224-142T=	ENSP00000497362.1:n.224-142T=
ENST00000258733.8:c.224-142T=	ENSP00000258733.4:n.224-142T=
ENST00000381990.6:c.224-142T=	ENSP00000371420.2:n.224-142T=
ENST00000409458.3:c.224-142T=	ENSP00000386476.3:n.224-142T=
ENST00000465673.5:n.402-142T=
ENST00000487890.5:n.415-142T=
ENST00000492512.1:n.304-142T=
ENST00000492858.6:n.426-142T=
NM_001005340.1:c.224-142T=	NP_001005340.1:n.224-142T=
NM_002510.2:c.224-142T=	NP_002501.1:n.224-142T=
XM_005249578.1:c.224-142T=	XP_005249635.1:n.224-142T=
XM_005249578.3:c.224-142T=	XP_005249635.1:n.224-142T=
XM_017011676.2:c.224-142T=	XP_016867165.1:n.224-142T=
XM_017011677.2:c.224-142T=	XP_016867166.1:n.224-142T=
XM_017011678.2:c.224-142T=	XP_016867167.1:n.224-142T=
NM_001005340.2:c.224-142T=	NP_001005340.1:n.224-142T=
NM_002510.3:c.224-142T= MANE Select	NP_002501.1:n.224-142T=