Canonical Allele Identifier: CA2579288533

Gene: DMRT1

Linked Data

• gnomAD v4: 9-894161-CTTA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.894163_894165del , CM000671.2:g.894163_894165del	GRCh38
NC_000009.11:g.894163_894165del , CM000671.1:g.894163_894165del	GRCh37
NC_000009.10:g.884163_884165del	NCBI36
NG_009221.1:g.57474_57476del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382276.8:c.790_792del MANE Select	ENSP00000371711.3:p.Tyr264del
ENST00000382276.7:c.790_792del	ENSP00000371711.3:p.Tyr264del
ENST00000564322.1:n.939_941del
ENST00000569227.1:c.316_318del	ENSP00000454701.1:p.Tyr106del
NM_021951.2:c.790_792del	NP_068770.2:p.Tyr264del
XM_006716732.1:c.790_792del	XP_006716795.1:p.Tyr264del
XM_011517770.1:c.838_840del	XP_011516072.1:p.Tyr280del
XM_011517771.1:c.838_840del	XP_011516073.1:p.Tyr280del
XM_011517772.1:c.838_840del	XP_011516074.1:p.Tyr280del
XM_011517773.1:c.316_318del	XP_011516075.1:p.Tyr106del
NM_001363767.1:c.316_318del	NP_001350696.1:p.Tyr106del
XM_011517773.3:c.316_318del	XP_011516075.1:p.Tyr106del
XM_017014374.1:c.587-22600_587-22598del	XP_016869863.1:n.587-22600_587-22598del
XM_017014375.1:c.539-22600_539-22598del	XP_016869864.1:n.539-22600_539-22598del
XM_024447434.1:c.244_246del	XP_024303202.1:p.Tyr82del
NM_021951.3:c.790_792del MANE Select	NP_068770.2:p.Tyr264del