Canonical Allele Identifier: CA1120422121

Gene: DMRT1

Linked Data

• dbSNP Id: rs1817263932
• gnomAD v3: 9-894204-T-C
• gnomAD v4: 9-894204-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.894204T>C , CM000671.2:g.894204T>C	GRCh38
NC_000009.11:g.894204T>C , CM000671.1:g.894204T>C	GRCh37
NC_000009.10:g.884204T>C	NCBI36
NG_009221.1:g.57515T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382276.8:c.822+9T>C MANE Select	ENSP00000371711.3:n.822+9T>C
ENST00000382276.7:c.822+9T>C	ENSP00000371711.3:n.822+9T>C
ENST00000564322.1:n.980T>C
ENST00000569227.1:c.348+9T>C	ENSP00000454701.1:n.348+9T>C
NM_021951.2:c.822+9T>C	NP_068770.2:n.822+9T>C
XM_006716732.1:c.822+9T>C	XP_006716795.1:n.822+9T>C
XM_011517770.1:c.870+9T>C	XP_011516072.1:n.870+9T>C
XM_011517771.1:c.870+9T>C	XP_011516073.1:n.870+9T>C
XM_011517772.1:c.870+9T>C	XP_011516074.1:n.870+9T>C
XM_011517773.1:c.348+9T>C	XP_011516075.1:n.348+9T>C
NM_001363767.1:c.348+9T>C	NP_001350696.1:n.348+9T>C
XM_011517773.3:c.348+9T>C	XP_011516075.1:n.348+9T>C
XM_017014374.1:c.587-22559T>C	XP_016869863.1:n.587-22559T>C
XM_017014375.1:c.539-22559T>C	XP_016869864.1:n.539-22559T>C
XM_024447434.1:c.276+9T>C	XP_024303202.1:n.276+9T>C
NM_021951.3:c.822+9T>C MANE Select	NP_068770.2:n.822+9T>C