Canonical Allele Identifier: CA187865455

Gene: DMRT1

Linked Data

• dbSNP Id: rs898896244
• gnomAD v2: 9-894326-GT-G
• gnomAD v3: 9-894326-GT-G
• gnomAD v4: 9-894326-GT-G
• MyVariant Identifiers: chr9:g.894327del (hg19) ; chr9:g.894327del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.894327del , CM000671.2:g.894327del	GRCh38
NC_000009.11:g.894327del , CM000671.1:g.894327del	GRCh37
NC_000009.10:g.884327del	NCBI36
NG_009221.1:g.57638del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382276.8:c.822+132del MANE Select	ENSP00000371711.3:n.822+132del
ENST00000382276.7:c.822+132del	ENSP00000371711.3:n.822+132del
ENST00000564322.1:n.1103del
ENST00000569227.1:c.348+132del	ENSP00000454701.1:n.348+132del
NM_021951.2:c.822+132del	NP_068770.2:n.822+132del
XM_006716732.1:c.822+132del	XP_006716795.1:n.822+132del
XM_011517770.1:c.870+132del	XP_011516072.1:n.870+132del
XM_011517771.1:c.870+132del	XP_011516073.1:n.870+132del
XM_011517772.1:c.870+132del	XP_011516074.1:n.870+132del
XM_011517773.1:c.348+132del	XP_011516075.1:n.348+132del
NM_001363767.1:c.348+132del	NP_001350696.1:n.348+132del
XM_011517773.3:c.348+132del	XP_011516075.1:n.348+132del
XM_017014374.1:c.587-22436del	XP_016869863.1:n.587-22436del
XM_017014375.1:c.539-22436del	XP_016869864.1:n.539-22436del
XM_024447434.1:c.276+132del	XP_024303202.1:n.276+132del
NM_021951.3:c.822+132del MANE Select	NP_068770.2:n.822+132del