Canonical Allele Identifier: CA372776389

Gene: DMRT1

Linked Data

• dbSNP Id: rs1817248713
• MyVariant Identifiers: chr9:g.893947A>T (hg19) ; chr9:g.893947A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.893947A>T , CM000671.2:g.893947A>T	GRCh38
NC_000009.11:g.893947A>T , CM000671.1:g.893947A>T	GRCh37
NC_000009.10:g.883947A>T	NCBI36
NG_009221.1:g.57258A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000382276.8:c.574A>T MANE Select	ENSP00000371711.3:p.Thr192Ser
ENST00000382276.7:c.574A>T	ENSP00000371711.3:p.Thr192Ser
ENST00000564322.1:n.723A>T
ENST00000569227.1:c.100A>T	ENSP00000454701.1:p.Thr34Ser
NM_021951.2:c.574A>T	NP_068770.2:p.Thr192Ser
XM_006716732.1:c.574A>T	XP_006716795.1:p.Thr192Ser
XM_011517770.1:c.622A>T	XP_011516072.1:p.Thr208Ser
XM_011517771.1:c.622A>T	XP_011516073.1:p.Thr208Ser
XM_011517772.1:c.622A>T	XP_011516074.1:p.Thr208Ser
XM_011517773.1:c.100A>T	XP_011516075.1:p.Thr34Ser
NM_001363767.1:c.100A>T	NP_001350696.1:p.Thr34Ser
XM_011517773.3:c.100A>T	XP_011516075.1:p.Thr34Ser
XM_017014374.1:c.587-22816A>T	XP_016869863.1:n.587-22816A>T
XM_017014375.1:c.539-22816A>T	XP_016869864.1:n.539-22816A>T
XM_024447434.1:c.28A>T	XP_024303202.1:p.Thr10Ser
NM_021951.3:c.574A>T MANE Select	NP_068770.2:p.Thr192Ser