Canonical Allele Identifier: CA1827191108

Gene: DMRT1

Linked Data

• dbSNP Id: rs1817271033

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.894341_894377del , CM000671.2:g.894341_894377del	GRCh38
NC_000009.11:g.894341_894377del , CM000671.1:g.894341_894377del	GRCh37
NC_000009.10:g.884341_884377del	NCBI36
NG_009221.1:g.57652_57688del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382276.8:c.822+146_822+182del MANE Select	ENSP00000371711.3:n.822+146_822+182del
ENST00000382276.7:c.822+146_822+182del	ENSP00000371711.3:n.822+146_822+182del
ENST00000564322.1:n.1117_1153del
ENST00000569227.1:c.348+146_348+182del	ENSP00000454701.1:n.348+146_348+182del
NM_021951.2:c.822+146_822+182del	NP_068770.2:n.822+146_822+182del
XM_006716732.1:c.822+146_822+182del	XP_006716795.1:n.822+146_822+182del
XM_011517770.1:c.870+146_870+182del	XP_011516072.1:n.870+146_870+182del
XM_011517771.1:c.870+146_870+182del	XP_011516073.1:n.870+146_870+182del
XM_011517772.1:c.870+146_870+182del	XP_011516074.1:n.870+146_870+182del
XM_011517773.1:c.348+146_348+182del	XP_011516075.1:n.348+146_348+182del
NM_001363767.1:c.348+146_348+182del	NP_001350696.1:n.348+146_348+182del
XM_011517773.3:c.348+146_348+182del	XP_011516075.1:n.348+146_348+182del
XM_017014374.1:c.587-22422_587-22386del	XP_016869863.1:n.587-22422_587-22386del
XM_017014375.1:c.539-22422_539-22386del	XP_016869864.1:n.539-22422_539-22386del
XM_024447434.1:c.276+146_276+182del	XP_024303202.1:n.276+146_276+182del
NM_021951.3:c.822+146_822+182del MANE Select	NP_068770.2:n.822+146_822+182del