Canonical Allele Identifier: CA372777066

Gene: DMRT1

Linked Data

• MyVariant Identifiers: chr9:g.894148G>A (hg19) ; chr9:g.894148G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.894148G>A , CM000671.2:g.894148G>A	GRCh38
NC_000009.11:g.894148G>A , CM000671.1:g.894148G>A	GRCh37
NC_000009.10:g.884148G>A	NCBI36
NG_009221.1:g.57459G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382276.8:c.775G>A MANE Select	ENSP00000371711.3:p.Gly259Ser
ENST00000382276.7:c.775G>A	ENSP00000371711.3:p.Gly259Ser
ENST00000564322.1:n.924G>A
ENST00000569227.1:c.301G>A	ENSP00000454701.1:p.Gly101Ser
NM_021951.2:c.775G>A	NP_068770.2:p.Gly259Ser
XM_006716732.1:c.775G>A	XP_006716795.1:p.Gly259Ser
XM_011517770.1:c.823G>A	XP_011516072.1:p.Gly275Ser
XM_011517771.1:c.823G>A	XP_011516073.1:p.Gly275Ser
XM_011517772.1:c.823G>A	XP_011516074.1:p.Gly275Ser
XM_011517773.1:c.301G>A	XP_011516075.1:p.Gly101Ser
NM_001363767.1:c.301G>A	NP_001350696.1:p.Gly101Ser
XM_011517773.3:c.301G>A	XP_011516075.1:p.Gly101Ser
XM_017014374.1:c.587-22615G>A	XP_016869863.1:n.587-22615G>A
XM_017014375.1:c.539-22615G>A	XP_016869864.1:n.539-22615G>A
XM_024447434.1:c.229G>A	XP_024303202.1:p.Gly77Ser
NM_021951.3:c.775G>A MANE Select	NP_068770.2:p.Gly259Ser