Canonical Allele Identifier: CA1694388121

Gene: GPNMB

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.23254153_23254154delinsCT , CM000669.2:g.23254153_23254154delinsCT	GRCh38
NC_000007.13:g.23293772_23293773delinsCT , CM000669.1:g.23293772_23293773delinsCT	GRCh37
NC_000007.12:g.23260297_23260298delinsCT	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000258733.9:c.224-16_224-15delinsCT MANE Select	ENSP00000258733.5:n.224-16_224-15delinsCT...
ENST00000647578.1:c.224-16_224-15delinsCT	ENSP00000497362.1:n.224-16_224-15delinsCT...
ENST00000258733.8:c.224-16_224-15delinsCT	ENSP00000258733.4:n.224-16_224-15delinsCT...
ENST00000381990.6:c.224-16_224-15delinsCT	ENSP00000371420.2:n.224-16_224-15delinsCT...
ENST00000409458.3:c.224-16_224-15delinsCT	ENSP00000386476.3:n.224-16_224-15delinsCT...
ENST00000465673.5:n.402-16_402-15delinsCT
ENST00000487890.5:n.415-16_415-15delinsCT
ENST00000492512.1:n.304-16_304-15delinsCT
ENST00000492858.6:n.426-16_426-15delinsCT
NM_001005340.1:c.224-16_224-15delinsCT	NP_001005340.1:n.224-16_224-15delinsCT
NM_002510.2:c.224-16_224-15delinsCT	NP_002501.1:n.224-16_224-15delinsCT
XM_005249578.1:c.224-16_224-15delinsCT	XP_005249635.1:n.224-16_224-15delinsCT
XM_005249578.3:c.224-16_224-15delinsCT	XP_005249635.1:n.224-16_224-15delinsCT
XM_017011676.2:c.224-16_224-15delinsCT	XP_016867165.1:n.224-16_224-15delinsCT
XM_017011677.2:c.224-16_224-15delinsCT	XP_016867166.1:n.224-16_224-15delinsCT
XM_017011678.2:c.224-16_224-15delinsCT	XP_016867167.1:n.224-16_224-15delinsCT
NM_001005340.2:c.224-16_224-15delinsCT	NP_001005340.1:n.224-16_224-15delinsCT
NM_002510.3:c.224-16_224-15delinsCT MANE Select	NP_002501.1:n.224-16_224-15delinsCT