Canonical Allele Identifier: CA1827190590

Gene: DMRT1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.893942C= , CM000671.2:g.893942C=	GRCh38
NC_000009.11:g.893942C= , CM000671.1:g.893942C=	GRCh37
NC_000009.10:g.883942C=	NCBI36
NG_009221.1:g.57253C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382276.8:c.569C= MANE Select	ENSP00000371711.3:p.Ala190=
ENST00000382276.7:c.569C=	ENSP00000371711.3:p.Ala190=
ENST00000564322.1:n.718C=
ENST00000569227.1:c.95C=	ENSP00000454701.1:p.Ala32=
NM_021951.2:c.569C=	NP_068770.2:p.Ala190=
XM_006716732.1:c.569C=	XP_006716795.1:p.Ala190=
XM_011517770.1:c.617C=	XP_011516072.1:p.Ala206=
XM_011517771.1:c.617C=	XP_011516073.1:p.Ala206=
XM_011517772.1:c.617C=	XP_011516074.1:p.Ala206=
XM_011517773.1:c.95C=	XP_011516075.1:p.Ala32=
NM_001363767.1:c.95C=	NP_001350696.1:p.Ala32=
XM_011517773.3:c.95C=	XP_011516075.1:p.Ala32=
XM_017014374.1:c.587-22821C=	XP_016869863.1:n.587-22821C=
XM_017014375.1:c.539-22821C=	XP_016869864.1:n.539-22821C=
XM_024447434.1:c.23C=	XP_024303202.1:p.Ala8=
NM_021951.3:c.569C= MANE Select	NP_068770.2:p.Ala190=