Canonical Allele Identifier: CA2689223605
Gene: DMRT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.894315_894327del , CM000671.2:g.894315_894327del GRCh38
NC_000009.11:g.894315_894327del , CM000671.1:g.894315_894327del GRCh37
NC_000009.10:g.884315_884327del NCBI36
NG_009221.1:g.57626_57638del

Transcript Alleles

HGVS Amino-acid Change
ENST00000382276.8:c.822+120_822+132del MANE Select ENSP00000371711.3:n.822+120_822+132del
ENST00000382276.7:c.822+120_822+132del ENSP00000371711.3:n.822+120_822+132del
ENST00000564322.1:n.1091_1103del
ENST00000569227.1:c.348+120_348+132del ENSP00000454701.1:n.348+120_348+132del
NM_021951.2:c.822+120_822+132del NP_068770.2:n.822+120_822+132del
XM_006716732.1:c.822+120_822+132del XP_006716795.1:n.822+120_822+132del
XM_011517770.1:c.870+120_870+132del XP_011516072.1:n.870+120_870+132del
XM_011517771.1:c.870+120_870+132del XP_011516073.1:n.870+120_870+132del
XM_011517772.1:c.870+120_870+132del XP_011516074.1:n.870+120_870+132del
XM_011517773.1:c.348+120_348+132del XP_011516075.1:n.348+120_348+132del
NM_001363767.1:c.348+120_348+132del NP_001350696.1:n.348+120_348+132del
XM_011517773.3:c.348+120_348+132del XP_011516075.1:n.348+120_348+132del
XM_017014374.1:c.587-22448_587-22436del XP_016869863.1:n.587-22448_587-22436del
XM_017014375.1:c.539-22448_539-22436del XP_016869864.1:n.539-22448_539-22436del
XM_024447434.1:c.276+120_276+132del XP_024303202.1:n.276+120_276+132del
NM_021951.3:c.822+120_822+132del MANE Select NP_068770.2:n.822+120_822+132del