Canonical Allele Identifier: CA2689223680
Gene: DMRT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.894345_894348dup , CM000671.2:g.894345_894348dup GRCh38
NC_000009.11:g.894345_894348dup , CM000671.1:g.894345_894348dup GRCh37
NC_000009.10:g.884345_884348dup NCBI36
NG_009221.1:g.57656_57659dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000382276.8:c.822+150_822+153dup MANE Select ENSP00000371711.3:n.822+150_822+153dup
ENST00000382276.7:c.822+150_822+153dup ENSP00000371711.3:n.822+150_822+153dup
ENST00000564322.1:n.1121_1124dup
ENST00000569227.1:c.348+150_348+153dup ENSP00000454701.1:n.348+150_348+153dup
NM_021951.2:c.822+150_822+153dup NP_068770.2:n.822+150_822+153dup
XM_006716732.1:c.822+150_822+153dup XP_006716795.1:n.822+150_822+153dup
XM_011517770.1:c.870+150_870+153dup XP_011516072.1:n.870+150_870+153dup
XM_011517771.1:c.870+150_870+153dup XP_011516073.1:n.870+150_870+153dup
XM_011517772.1:c.870+150_870+153dup XP_011516074.1:n.870+150_870+153dup
XM_011517773.1:c.348+150_348+153dup XP_011516075.1:n.348+150_348+153dup
NM_001363767.1:c.348+150_348+153dup NP_001350696.1:n.348+150_348+153dup
XM_011517773.3:c.348+150_348+153dup XP_011516075.1:n.348+150_348+153dup
XM_017014374.1:c.587-22418_587-22415dup XP_016869863.1:n.587-22418_587-22415dup
XM_017014375.1:c.539-22418_539-22415dup XP_016869864.1:n.539-22418_539-22415dup
XM_024447434.1:c.276+150_276+153dup XP_024303202.1:n.276+150_276+153dup
NM_021951.3:c.822+150_822+153dup MANE Select NP_068770.2:n.822+150_822+153dup