Canonical Allele Identifier: CA372776556

Gene: DMRT1

Linked Data

• dbSNP Id: rs1586579116
• MyVariant Identifiers: chr9:g.893995A>C (hg19) ; chr9:g.893995A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.893995A>C , CM000671.2:g.893995A>C	GRCh38
NC_000009.11:g.893995A>C , CM000671.1:g.893995A>C	GRCh37
NC_000009.10:g.883995A>C	NCBI36
NG_009221.1:g.57306A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382276.8:c.622A>C MANE Select	ENSP00000371711.3:p.Thr208Pro
ENST00000382276.7:c.622A>C	ENSP00000371711.3:p.Thr208Pro
ENST00000564322.1:n.771A>C
ENST00000569227.1:c.148A>C	ENSP00000454701.1:p.Thr50Pro
NM_021951.2:c.622A>C	NP_068770.2:p.Thr208Pro
XM_006716732.1:c.622A>C	XP_006716795.1:p.Thr208Pro
XM_011517770.1:c.670A>C	XP_011516072.1:p.Thr224Pro
XM_011517771.1:c.670A>C	XP_011516073.1:p.Thr224Pro
XM_011517772.1:c.670A>C	XP_011516074.1:p.Thr224Pro
XM_011517773.1:c.148A>C	XP_011516075.1:p.Thr50Pro
NM_001363767.1:c.148A>C	NP_001350696.1:p.Thr50Pro
XM_011517773.3:c.148A>C	XP_011516075.1:p.Thr50Pro
XM_017014374.1:c.587-22768A>C	XP_016869863.1:n.587-22768A>C
XM_017014375.1:c.539-22768A>C	XP_016869864.1:n.539-22768A>C
XM_024447434.1:c.76A>C	XP_024303202.1:p.Thr26Pro
NM_021951.3:c.622A>C MANE Select	NP_068770.2:p.Thr208Pro