Canonical Allele Identifier: CA4961662

Gene: DMRT1

Linked Data

• dbSNP Id: rs774678938
• ExAC: 9:894176 A / AGACAGG
• gnomAD v2: 9-894176-A-AGACAGG
• gnomAD v4: 9-894176-A-AGACAGG
• MyVariant Identifiers: chr9:g.894176_894177insGACAGG (hg19) ; chr9:g.894176_894177insGACAGG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.894177_894182dup , CM000671.2:g.894177_894182dup	GRCh38
NC_000009.11:g.894177_894182dup , CM000671.1:g.894177_894182dup	GRCh37
NC_000009.10:g.884177_884182dup	NCBI36
NG_009221.1:g.57488_57493dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382276.8:c.804_809dup MANE Select	ENSP00000371711.3:p.Gly270_Asn271insThrGly
ENST00000382276.7:c.804_809dup	ENSP00000371711.3:p.Gly270_Asn271insThrGly
ENST00000564322.1:n.953_958dup
ENST00000569227.1:c.330_335dup	ENSP00000454701.1:p.Gly112_Asn113insThrGly
NM_021951.2:c.804_809dup	NP_068770.2:p.Gly270_Asn271insThrGly
XM_006716732.1:c.804_809dup	XP_006716795.1:p.Gly270_Asn271insThrGly
XM_011517770.1:c.852_857dup	XP_011516072.1:p.Gly286_Asn287insThrGly
XM_011517771.1:c.852_857dup	XP_011516073.1:p.Gly286_Asn287insThrGly
XM_011517772.1:c.852_857dup	XP_011516074.1:p.Gly286_Asn287insThrGly
XM_011517773.1:c.330_335dup	XP_011516075.1:p.Gly112_Asn113insThrGly
NM_001363767.1:c.330_335dup	NP_001350696.1:p.Gly112_Asn113insThrGly
XM_011517773.3:c.330_335dup	XP_011516075.1:p.Gly112_Asn113insThrGly
XM_017014374.1:c.587-22586_587-22581dup	XP_016869863.1:n.587-22586_587-22581dup
XM_017014375.1:c.539-22586_539-22581dup	XP_016869864.1:n.539-22586_539-22581dup
XM_024447434.1:c.258_263dup	XP_024303202.1:p.Gly88_Asn89insThrGly
NM_021951.3:c.804_809dup MANE Select	NP_068770.2:p.Gly270_Asn271insThrGly