Canonical Allele Identifier: CA463850477

Gene: DMRT1

Linked Data

• gnomAD v4: 9-894123-A-T
• MyVariant Identifiers: chr9:g.894123A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.894123A>T , CM000671.2:g.894123A>T	GRCh38
NC_000009.11:g.894123A>T , CM000671.1:g.894123A>T	GRCh37
NC_000009.10:g.884123A>T	NCBI36
NG_009221.1:g.57434A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382276.8:c.750A>T MANE Select	ENSP00000371711.3:p.Gly250=
ENST00000382276.7:c.750A>T	ENSP00000371711.3:p.Gly250=
ENST00000564322.1:n.899A>T
ENST00000569227.1:c.276A>T	ENSP00000454701.1:p.Gly92=
NM_021951.2:c.750A>T	NP_068770.2:p.Gly250=
XM_006716732.1:c.750A>T	XP_006716795.1:p.Gly250=
XM_011517770.1:c.798A>T	XP_011516072.1:p.Gly266=
XM_011517771.1:c.798A>T	XP_011516073.1:p.Gly266=
XM_011517772.1:c.798A>T	XP_011516074.1:p.Gly266=
XM_011517773.1:c.276A>T	XP_011516075.1:p.Gly92=
NM_001363767.1:c.276A>T	NP_001350696.1:p.Gly92=
XM_011517773.3:c.276A>T	XP_011516075.1:p.Gly92=
XM_017014374.1:c.587-22640A>T	XP_016869863.1:n.587-22640A>T
XM_017014375.1:c.539-22640A>T	XP_016869864.1:n.539-22640A>T
XM_024447434.1:c.204A>T	XP_024303202.1:p.Gly68=
NM_021951.3:c.750A>T MANE Select	NP_068770.2:p.Gly250=