Canonical Allele Identifier: CA463850289

Gene: DMRT1

Linked Data

• MyVariant Identifiers: chr9:g.893949C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.893949C>T , CM000671.2:g.893949C>T	GRCh38
NC_000009.11:g.893949C>T , CM000671.1:g.893949C>T	GRCh37
NC_000009.10:g.883949C>T	NCBI36
NG_009221.1:g.57260C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000382276.8:c.576C>T MANE Select	ENSP00000371711.3:p.Thr192=
ENST00000382276.7:c.576C>T	ENSP00000371711.3:p.Thr192=
ENST00000564322.1:n.725C>T
ENST00000569227.1:c.102C>T	ENSP00000454701.1:p.Thr34=
NM_021951.2:c.576C>T	NP_068770.2:p.Thr192=
XM_006716732.1:c.576C>T	XP_006716795.1:p.Thr192=
XM_011517770.1:c.624C>T	XP_011516072.1:p.Thr208=
XM_011517771.1:c.624C>T	XP_011516073.1:p.Thr208=
XM_011517772.1:c.624C>T	XP_011516074.1:p.Thr208=
XM_011517773.1:c.102C>T	XP_011516075.1:p.Thr34=
NM_001363767.1:c.102C>T	NP_001350696.1:p.Thr34=
XM_011517773.3:c.102C>T	XP_011516075.1:p.Thr34=
XM_017014374.1:c.587-22814C>T	XP_016869863.1:n.587-22814C>T
XM_017014375.1:c.539-22814C>T	XP_016869864.1:n.539-22814C>T
XM_024447434.1:c.30C>T	XP_024303202.1:p.Thr10=
NM_021951.3:c.576C>T MANE Select	NP_068770.2:p.Thr192=