Canonical Allele Identifier: CA372777075

Gene: DMRT1

Linked Data

• gnomAD v4: 9-894149-G-C
• MyVariant Identifiers: chr9:g.894149G>C (hg19) ; chr9:g.894149G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.894149G>C , CM000671.2:g.894149G>C	GRCh38
NC_000009.11:g.894149G>C , CM000671.1:g.894149G>C	GRCh37
NC_000009.10:g.884149G>C	NCBI36
NG_009221.1:g.57460G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382276.8:c.776G>C MANE Select	ENSP00000371711.3:p.Gly259Ala
ENST00000382276.7:c.776G>C	ENSP00000371711.3:p.Gly259Ala
ENST00000564322.1:n.925G>C
ENST00000569227.1:c.302G>C	ENSP00000454701.1:p.Gly101Ala
NM_021951.2:c.776G>C	NP_068770.2:p.Gly259Ala
XM_006716732.1:c.776G>C	XP_006716795.1:p.Gly259Ala
XM_011517770.1:c.824G>C	XP_011516072.1:p.Gly275Ala
XM_011517771.1:c.824G>C	XP_011516073.1:p.Gly275Ala
XM_011517772.1:c.824G>C	XP_011516074.1:p.Gly275Ala
XM_011517773.1:c.302G>C	XP_011516075.1:p.Gly101Ala
NM_001363767.1:c.302G>C	NP_001350696.1:p.Gly101Ala
XM_011517773.3:c.302G>C	XP_011516075.1:p.Gly101Ala
XM_017014374.1:c.587-22614G>C	XP_016869863.1:n.587-22614G>C
XM_017014375.1:c.539-22614G>C	XP_016869864.1:n.539-22614G>C
XM_024447434.1:c.230G>C	XP_024303202.1:p.Gly77Ala
NM_021951.3:c.776G>C MANE Select	NP_068770.2:p.Gly259Ala