Canonical Allele Identifier: CA372777073

Gene: DMRT1

Linked Data

• dbSNP Id: rs772743162
• gnomAD v2: 9-894149-G-A
• gnomAD v4: 9-894149-G-A
• MyVariant Identifiers: chr9:g.894149G>A (hg19) ; chr9:g.894149G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.894149G>A , CM000671.2:g.894149G>A	GRCh38
NC_000009.11:g.894149G>A , CM000671.1:g.894149G>A	GRCh37
NC_000009.10:g.884149G>A	NCBI36
NG_009221.1:g.57460G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382276.8:c.776G>A MANE Select	ENSP00000371711.3:p.Gly259Asp
ENST00000382276.7:c.776G>A	ENSP00000371711.3:p.Gly259Asp
ENST00000564322.1:n.925G>A
ENST00000569227.1:c.302G>A	ENSP00000454701.1:p.Gly101Asp
NM_021951.2:c.776G>A	NP_068770.2:p.Gly259Asp
XM_006716732.1:c.776G>A	XP_006716795.1:p.Gly259Asp
XM_011517770.1:c.824G>A	XP_011516072.1:p.Gly275Asp
XM_011517771.1:c.824G>A	XP_011516073.1:p.Gly275Asp
XM_011517772.1:c.824G>A	XP_011516074.1:p.Gly275Asp
XM_011517773.1:c.302G>A	XP_011516075.1:p.Gly101Asp
NM_001363767.1:c.302G>A	NP_001350696.1:p.Gly101Asp
XM_011517773.3:c.302G>A	XP_011516075.1:p.Gly101Asp
XM_017014374.1:c.587-22614G>A	XP_016869863.1:n.587-22614G>A
XM_017014375.1:c.539-22614G>A	XP_016869864.1:n.539-22614G>A
XM_024447434.1:c.230G>A	XP_024303202.1:p.Gly77Asp
NM_021951.3:c.776G>A MANE Select	NP_068770.2:p.Gly259Asp