Canonical Allele Identifier: CA1827191104

Gene: DMRT1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.894335_894339delinsCATAT , CM000671.2:g.894335_894339delinsCATAT	GRCh38
NC_000009.11:g.894335_894339delinsCATAT , CM000671.1:g.894335_894339delinsCATAT	GRCh37
NC_000009.10:g.884335_884339delinsCATAT	NCBI36
NG_009221.1:g.57646_57650delinsCATAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382276.8:c.822+140_822+144delinsCATAT MANE Select	ENSP00000371711.3:n.822+140_822+144delinsCATAT
ENST00000382276.7:c.822+140_822+144delinsCATAT	ENSP00000371711.3:n.822+140_822+144delinsCATAT
ENST00000564322.1:n.1111_1115delinsCATAT
ENST00000569227.1:c.348+140_348+144delinsCATAT	ENSP00000454701.1:n.348+140_348+144delinsCATAT
NM_021951.2:c.822+140_822+144delinsCATAT	NP_068770.2:n.822+140_822+144delinsCATAT
XM_006716732.1:c.822+140_822+144delinsCATAT	XP_006716795.1:n.822+140_822+144delinsCATAT
XM_011517770.1:c.870+140_870+144delinsCATAT	XP_011516072.1:n.870+140_870+144delinsCATAT
XM_011517771.1:c.870+140_870+144delinsCATAT	XP_011516073.1:n.870+140_870+144delinsCATAT
XM_011517772.1:c.870+140_870+144delinsCATAT	XP_011516074.1:n.870+140_870+144delinsCATAT
XM_011517773.1:c.348+140_348+144delinsCATAT	XP_011516075.1:n.348+140_348+144delinsCATAT
NM_001363767.1:c.348+140_348+144delinsCATAT	NP_001350696.1:n.348+140_348+144delinsCATAT
XM_011517773.3:c.348+140_348+144delinsCATAT	XP_011516075.1:n.348+140_348+144delinsCATAT
XM_017014374.1:c.587-22428_587-22424delinsCATAT	XP_016869863.1:n.587-22428_587-22424delinsCATAT
XM_017014375.1:c.539-22428_539-22424delinsCATAT	XP_016869864.1:n.539-22428_539-22424delinsCATAT
XM_024447434.1:c.276+140_276+144delinsCATAT	XP_024303202.1:n.276+140_276+144delinsCATAT
NM_021951.3:c.822+140_822+144delinsCATAT MANE Select	NP_068770.2:n.822+140_822+144delinsCATAT