Canonical Allele Identifier: CA2689223626
Gene: DMRT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.894325_894336dup , CM000671.2:g.894325_894336dup GRCh38
NC_000009.11:g.894325_894336dup , CM000671.1:g.894325_894336dup GRCh37
NC_000009.10:g.884325_884336dup NCBI36
NG_009221.1:g.57636_57647dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000382276.8:c.822+130_822+141dup MANE Select ENSP00000371711.3:n.822+130_822+141dup
ENST00000382276.7:c.822+130_822+141dup ENSP00000371711.3:n.822+130_822+141dup
ENST00000564322.1:n.1101_1112dup
ENST00000569227.1:c.348+130_348+141dup ENSP00000454701.1:n.348+130_348+141dup
NM_021951.2:c.822+130_822+141dup NP_068770.2:n.822+130_822+141dup
XM_006716732.1:c.822+130_822+141dup XP_006716795.1:n.822+130_822+141dup
XM_011517770.1:c.870+130_870+141dup XP_011516072.1:n.870+130_870+141dup
XM_011517771.1:c.870+130_870+141dup XP_011516073.1:n.870+130_870+141dup
XM_011517772.1:c.870+130_870+141dup XP_011516074.1:n.870+130_870+141dup
XM_011517773.1:c.348+130_348+141dup XP_011516075.1:n.348+130_348+141dup
NM_001363767.1:c.348+130_348+141dup NP_001350696.1:n.348+130_348+141dup
XM_011517773.3:c.348+130_348+141dup XP_011516075.1:n.348+130_348+141dup
XM_017014374.1:c.587-22438_587-22427dup XP_016869863.1:n.587-22438_587-22427dup
XM_017014375.1:c.539-22438_539-22427dup XP_016869864.1:n.539-22438_539-22427dup
XM_024447434.1:c.276+130_276+141dup XP_024303202.1:n.276+130_276+141dup
NM_021951.3:c.822+130_822+141dup MANE Select NP_068770.2:n.822+130_822+141dup