Canonical Allele Identifier: CA372776964

Gene: DMRT1

Linked Data

• MyVariant Identifiers: chr9:g.894113C>G (hg19) ; chr9:g.894113C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.894113C>G , CM000671.2:g.894113C>G	GRCh38
NC_000009.11:g.894113C>G , CM000671.1:g.894113C>G	GRCh37
NC_000009.10:g.884113C>G	NCBI36
NG_009221.1:g.57424C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382276.8:c.740C>G MANE Select	ENSP00000371711.3:p.Pro247Arg
ENST00000382276.7:c.740C>G	ENSP00000371711.3:p.Pro247Arg
ENST00000564322.1:n.889C>G
ENST00000569227.1:c.266C>G	ENSP00000454701.1:p.Pro89Arg
NM_021951.2:c.740C>G	NP_068770.2:p.Pro247Arg
XM_006716732.1:c.740C>G	XP_006716795.1:p.Pro247Arg
XM_011517770.1:c.788C>G	XP_011516072.1:p.Pro263Arg
XM_011517771.1:c.788C>G	XP_011516073.1:p.Pro263Arg
XM_011517772.1:c.788C>G	XP_011516074.1:p.Pro263Arg
XM_011517773.1:c.266C>G	XP_011516075.1:p.Pro89Arg
NM_001363767.1:c.266C>G	NP_001350696.1:p.Pro89Arg
XM_011517773.3:c.266C>G	XP_011516075.1:p.Pro89Arg
XM_017014374.1:c.587-22650C>G	XP_016869863.1:n.587-22650C>G
XM_017014375.1:c.539-22650C>G	XP_016869864.1:n.539-22650C>G
XM_024447434.1:c.194C>G	XP_024303202.1:p.Pro65Arg
NM_021951.3:c.740C>G MANE Select	NP_068770.2:p.Pro247Arg