Canonical Allele Identifier: CA2689223511
Gene: DMRT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.894248_894251dup , CM000671.2:g.894248_894251dup GRCh38
NC_000009.11:g.894248_894251dup , CM000671.1:g.894248_894251dup GRCh37
NC_000009.10:g.884248_884251dup NCBI36
NG_009221.1:g.57559_57562dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000382276.8:c.822+53_822+56dup MANE Select ENSP00000371711.3:n.822+53_822+56dup
ENST00000382276.7:c.822+53_822+56dup ENSP00000371711.3:n.822+53_822+56dup
ENST00000564322.1:n.1024_1027dup
ENST00000569227.1:c.348+53_348+56dup ENSP00000454701.1:n.348+53_348+56dup
NM_021951.2:c.822+53_822+56dup NP_068770.2:n.822+53_822+56dup
XM_006716732.1:c.822+53_822+56dup XP_006716795.1:n.822+53_822+56dup
XM_011517770.1:c.870+53_870+56dup XP_011516072.1:n.870+53_870+56dup
XM_011517771.1:c.870+53_870+56dup XP_011516073.1:n.870+53_870+56dup
XM_011517772.1:c.870+53_870+56dup XP_011516074.1:n.870+53_870+56dup
XM_011517773.1:c.348+53_348+56dup XP_011516075.1:n.348+53_348+56dup
NM_001363767.1:c.348+53_348+56dup NP_001350696.1:n.348+53_348+56dup
XM_011517773.3:c.348+53_348+56dup XP_011516075.1:n.348+53_348+56dup
XM_017014374.1:c.587-22515_587-22512dup XP_016869863.1:n.587-22515_587-22512dup
XM_017014375.1:c.539-22515_539-22512dup XP_016869864.1:n.539-22515_539-22512dup
XM_024447434.1:c.276+53_276+56dup XP_024303202.1:n.276+53_276+56dup
NM_021951.3:c.822+53_822+56dup MANE Select NP_068770.2:n.822+53_822+56dup