Canonical Allele Identifier: CA372776939

Gene: DMRT1

Linked Data

• gnomAD v4: 9-894106-G-A
• MyVariant Identifiers: chr9:g.894106G>A (hg19) ; chr9:g.894106G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.894106G>A , CM000671.2:g.894106G>A	GRCh38
NC_000009.11:g.894106G>A , CM000671.1:g.894106G>A	GRCh37
NC_000009.10:g.884106G>A	NCBI36
NG_009221.1:g.57417G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382276.8:c.733G>A MANE Select	ENSP00000371711.3:p.Gly245Arg
ENST00000382276.7:c.733G>A	ENSP00000371711.3:p.Gly245Arg
ENST00000564322.1:n.882G>A
ENST00000569227.1:c.259G>A	ENSP00000454701.1:p.Gly87Arg
NM_021951.2:c.733G>A	NP_068770.2:p.Gly245Arg
XM_006716732.1:c.733G>A	XP_006716795.1:p.Gly245Arg
XM_011517770.1:c.781G>A	XP_011516072.1:p.Gly261Arg
XM_011517771.1:c.781G>A	XP_011516073.1:p.Gly261Arg
XM_011517772.1:c.781G>A	XP_011516074.1:p.Gly261Arg
XM_011517773.1:c.259G>A	XP_011516075.1:p.Gly87Arg
NM_001363767.1:c.259G>A	NP_001350696.1:p.Gly87Arg
XM_011517773.3:c.259G>A	XP_011516075.1:p.Gly87Arg
XM_017014374.1:c.587-22657G>A	XP_016869863.1:n.587-22657G>A
XM_017014375.1:c.539-22657G>A	XP_016869864.1:n.539-22657G>A
XM_024447434.1:c.187G>A	XP_024303202.1:p.Gly63Arg
NM_021951.3:c.733G>A MANE Select	NP_068770.2:p.Gly245Arg