Canonical Allele Identifier: CA586167809

Gene: DMRT1

Linked Data

• dbSNP Id: rs1176707510
• gnomAD v2: 9-894330-ACACACATATGTGTGTGTGCCATTTTG-A
• gnomAD v3: 9-894330-ACACACATATGTGTGTGTGCCATTTTG-A
• gnomAD v4: 9-894330-ACACACATATGTGTGTGTGCCATTTTG-A
• MyVariant Identifiers: chr9:g.894331_894356del (hg19) ; chr9:g.894331_894356del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.894338_894363del , CM000671.2:g.894338_894363del	GRCh38
NC_000009.11:g.894338_894363del , CM000671.1:g.894338_894363del	GRCh37
NC_000009.10:g.884338_884363del	NCBI36
NG_009221.1:g.57649_57674del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382276.8:c.822+143_822+168del MANE Select	ENSP00000371711.3:n.822+143_822+168del
ENST00000382276.7:c.822+143_822+168del	ENSP00000371711.3:n.822+143_822+168del
ENST00000564322.1:n.1114_1139del
ENST00000569227.1:c.348+143_348+168del	ENSP00000454701.1:n.348+143_348+168del
NM_021951.2:c.822+143_822+168del	NP_068770.2:n.822+143_822+168del
XM_006716732.1:c.822+143_822+168del	XP_006716795.1:n.822+143_822+168del
XM_011517770.1:c.870+143_870+168del	XP_011516072.1:n.870+143_870+168del
XM_011517771.1:c.870+143_870+168del	XP_011516073.1:n.870+143_870+168del
XM_011517772.1:c.870+143_870+168del	XP_011516074.1:n.870+143_870+168del
XM_011517773.1:c.348+143_348+168del	XP_011516075.1:n.348+143_348+168del
NM_001363767.1:c.348+143_348+168del	NP_001350696.1:n.348+143_348+168del
XM_011517773.3:c.348+143_348+168del	XP_011516075.1:n.348+143_348+168del
XM_017014374.1:c.587-22425_587-22400del	XP_016869863.1:n.587-22425_587-22400del
XM_017014375.1:c.539-22425_539-22400del	XP_016869864.1:n.539-22425_539-22400del
XM_024447434.1:c.276+143_276+168del	XP_024303202.1:n.276+143_276+168del
NM_021951.3:c.822+143_822+168del MANE Select	NP_068770.2:n.822+143_822+168del