Canonical Allele Identifier: CA1827190605

Gene: DMRT1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.893958G= , CM000671.2:g.893958G=	GRCh38
NC_000009.11:g.893958G= , CM000671.1:g.893958G=	GRCh37
NC_000009.10:g.883958G=	NCBI36
NG_009221.1:g.57269G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000382276.8:c.585G= MANE Select	ENSP00000371711.3:p.Gly195=
ENST00000382276.7:c.585G=	ENSP00000371711.3:p.Gly195=
ENST00000564322.1:n.734G=
ENST00000569227.1:c.111G=	ENSP00000454701.1:p.Gly37=
NM_021951.2:c.585G=	NP_068770.2:p.Gly195=
XM_006716732.1:c.585G=	XP_006716795.1:p.Gly195=
XM_011517770.1:c.633G=	XP_011516072.1:p.Gly211=
XM_011517771.1:c.633G=	XP_011516073.1:p.Gly211=
XM_011517772.1:c.633G=	XP_011516074.1:p.Gly211=
XM_011517773.1:c.111G=	XP_011516075.1:p.Gly37=
NM_001363767.1:c.111G=	NP_001350696.1:p.Gly37=
XM_011517773.3:c.111G=	XP_011516075.1:p.Gly37=
XM_017014374.1:c.587-22805G=	XP_016869863.1:n.587-22805G=
XM_017014375.1:c.539-22805G=	XP_016869864.1:n.539-22805G=
XM_024447434.1:c.39G=	XP_024303202.1:p.Gly13=
NM_021951.3:c.585G= MANE Select	NP_068770.2:p.Gly195=