Canonical Allele Identifier: CA2682036557

Gene: GPNMB

Linked Data

• gnomAD v4: 7-23254065-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.23254065G>T , CM000669.2:g.23254065G>T	GRCh38
NC_000007.13:g.23293684G>T , CM000669.1:g.23293684G>T	GRCh37
NC_000007.12:g.23260209G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000258733.9:c.224-104G>T MANE Select	ENSP00000258733.5:n.224-104G>T
ENST00000647578.1:c.224-104G>T	ENSP00000497362.1:n.224-104G>T
ENST00000258733.8:c.224-104G>T	ENSP00000258733.4:n.224-104G>T
ENST00000381990.6:c.224-104G>T	ENSP00000371420.2:n.224-104G>T
ENST00000409458.3:c.224-104G>T	ENSP00000386476.3:n.224-104G>T
ENST00000465673.5:n.402-104G>T
ENST00000487890.5:n.415-104G>T
ENST00000492512.1:n.304-104G>T
ENST00000492858.6:n.426-104G>T
NM_001005340.1:c.224-104G>T	NP_001005340.1:n.224-104G>T
NM_002510.2:c.224-104G>T	NP_002501.1:n.224-104G>T
XM_005249578.1:c.224-104G>T	XP_005249635.1:n.224-104G>T
XM_005249578.3:c.224-104G>T	XP_005249635.1:n.224-104G>T
XM_017011676.2:c.224-104G>T	XP_016867165.1:n.224-104G>T
XM_017011677.2:c.224-104G>T	XP_016867166.1:n.224-104G>T
XM_017011678.2:c.224-104G>T	XP_016867167.1:n.224-104G>T
NM_001005340.2:c.224-104G>T	NP_001005340.1:n.224-104G>T
NM_002510.3:c.224-104G>T MANE Select	NP_002501.1:n.224-104G>T