Canonical Allele Identifier: CA372777228

Gene: DMRT1

Linked Data

• MyVariant Identifiers: chr9:g.894193C>T (hg19) ; chr9:g.894193C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.894193C>T , CM000671.2:g.894193C>T	GRCh38
NC_000009.11:g.894193C>T , CM000671.1:g.894193C>T	GRCh37
NC_000009.10:g.884193C>T	NCBI36
NG_009221.1:g.57504C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382276.8:c.820C>T MANE Select	ENSP00000371711.3:p.Gln274Ter
ENST00000382276.7:c.820C>T	ENSP00000371711.3:p.Gln274Ter
ENST00000564322.1:n.969C>T
ENST00000569227.1:c.346C>T	ENSP00000454701.1:p.Gln116Ter
NM_021951.2:c.820C>T	NP_068770.2:p.Gln274Ter
XM_006716732.1:c.820C>T	XP_006716795.1:p.Gln274Ter
XM_011517770.1:c.868C>T	XP_011516072.1:p.Gln290Ter
XM_011517771.1:c.868C>T	XP_011516073.1:p.Gln290Ter
XM_011517772.1:c.868C>T	XP_011516074.1:p.Gln290Ter
XM_011517773.1:c.346C>T	XP_011516075.1:p.Gln116Ter
NM_001363767.1:c.346C>T	NP_001350696.1:p.Gln116Ter
XM_011517773.3:c.346C>T	XP_011516075.1:p.Gln116Ter
XM_017014374.1:c.587-22570C>T	XP_016869863.1:n.587-22570C>T
XM_017014375.1:c.539-22570C>T	XP_016869864.1:n.539-22570C>T
XM_024447434.1:c.274C>T	XP_024303202.1:p.Gln92Ter
NM_021951.3:c.820C>T MANE Select	NP_068770.2:p.Gln274Ter