Canonical Allele Identifier: CA1827190593

Gene: DMRT1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.893944G= , CM000671.2:g.893944G=	GRCh38
NC_000009.11:g.893944G= , CM000671.1:g.893944G=	GRCh37
NC_000009.10:g.883944G=	NCBI36
NG_009221.1:g.57255G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000382276.8:c.571G= MANE Select	ENSP00000371711.3:p.Val191=
ENST00000382276.7:c.571G=	ENSP00000371711.3:p.Val191=
ENST00000564322.1:n.720G=
ENST00000569227.1:c.97G=	ENSP00000454701.1:p.Val33=
NM_021951.2:c.571G=	NP_068770.2:p.Val191=
XM_006716732.1:c.571G=	XP_006716795.1:p.Val191=
XM_011517770.1:c.619G=	XP_011516072.1:p.Val207=
XM_011517771.1:c.619G=	XP_011516073.1:p.Val207=
XM_011517772.1:c.619G=	XP_011516074.1:p.Val207=
XM_011517773.1:c.97G=	XP_011516075.1:p.Val33=
NM_001363767.1:c.97G=	NP_001350696.1:p.Val33=
XM_011517773.3:c.97G=	XP_011516075.1:p.Val33=
XM_017014374.1:c.587-22819G=	XP_016869863.1:n.587-22819G=
XM_017014375.1:c.539-22819G=	XP_016869864.1:n.539-22819G=
XM_024447434.1:c.25G=	XP_024303202.1:p.Val9=
NM_021951.3:c.571G= MANE Select	NP_068770.2:p.Val191=