Canonical Allele Identifier: CA4961749
Community Standard Title: NM_021951.3(DMRT1):c.968-34_968-27dup
Gene: DMRT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.967951_967958dup , CM000671.2:g.967951_967958dup GRCh38
NC_000009.11:g.967951_967958dup , CM000671.1:g.967951_967958dup GRCh37
NC_000009.10:g.957951_957958dup NCBI36
NG_009221.1:g.131262_131269dup

Transcript Alleles

HGVS Amino-acid Change
NM_021951.3:c.968-34_968-27dup MANE Select NP_068770.2:n.968-34_968-27dup
ENST00000382276.8:c.968-34_968-27dup MANE Select ENSP00000371711.3:n.968-34_968-27dup
NM_001363767.1:c.494-34_494-27dup NP_001350696.1:n.494-34_494-27dup
NM_021951.2:c.968-34_968-27dup NP_068770.2:n.968-34_968-27dup
ENST00000382276.7:c.968-34_968-27dup ENSP00000371711.3:n.968-34_968-27dup
ENST00000569227.1:c.494-34_494-27dup ENSP00000454701.1:n.494-34_494-27dup
XM_006716732.1:c.971-34_971-27dup XP_006716795.1:n.971-34_971-27dup
XM_011517770.1:c.1019-34_1019-27dup XP_011516072.1:n.1019-34_1019-27dup
XM_011517771.1:c.1016-34_1016-27dup XP_011516073.1:n.1016-34_1016-27dup
XM_011517772.1:c.871-34_871-27dup XP_011516074.1:n.871-34_871-27dup
XM_011517773.1:c.497-34_497-27dup XP_011516075.1:n.497-34_497-27dup
XM_011517773.3:c.497-34_497-27dup XP_011516075.1:n.497-34_497-27dup
XM_017014374.1:c.*36-34_*36-27dup XP_016869863.1:n.*36-34_*36-27dup
XM_017014375.1:c.*36-34_*36-27dup XP_016869864.1:n.*36-34_*36-27dup
XM_024447434.1:c.422-34_422-27dup XP_024303202.1:n.422-34_422-27dup