Canonical Allele Identifier: CA463850525

Gene: DMRT1

Linked Data

• COSMIC: COSM1463440
• MyVariant Identifiers: chr9:g.894146del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.894149del , CM000671.2:g.894149del	GRCh38
NC_000009.11:g.894149del , CM000671.1:g.894149del	GRCh37
NC_000009.10:g.884149del	NCBI36
NG_009221.1:g.57460del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382276.8:c.776del MANE Select	ENSP00000371711.3:p.Gly259AlafsTer17
ENST00000382276.7:c.776del	ENSP00000371711.3:p.Gly259AlafsTer17
ENST00000564322.1:n.925del
ENST00000569227.1:c.302del	ENSP00000454701.1:p.Gly101AlafsTer17
NM_021951.2:c.776del	NP_068770.2:p.Gly259AlafsTer17
XM_006716732.1:c.776del	XP_006716795.1:p.Gly259AlafsTer18
XM_011517770.1:c.824del	XP_011516072.1:p.Gly275AlafsTer18
XM_011517771.1:c.824del	XP_011516073.1:p.Gly275AlafsTer17
XM_011517772.1:c.824del	XP_011516074.1:p.Gly275AlafsTer?
XM_011517773.1:c.302del	XP_011516075.1:p.Gly101AlafsTer18
NM_001363767.1:c.302del	NP_001350696.1:p.Gly101AlafsTer17
XM_011517773.3:c.302del	XP_011516075.1:p.Gly101AlafsTer18
XM_017014374.1:c.587-22614del	XP_016869863.1:n.587-22614del
XM_017014375.1:c.539-22614del	XP_016869864.1:n.539-22614del
XM_024447434.1:c.230del	XP_024303202.1:p.Gly77AlafsTer17
NM_021951.3:c.776del MANE Select	NP_068770.2:p.Gly259AlafsTer17