Canonical Allele Identifier: CA1827191114

Gene: DMRT1

Linked Data

• dbSNP Id: rs1817271169

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.894338_894341del , CM000671.2:g.894338_894341del	GRCh38
NC_000009.11:g.894338_894341del , CM000671.1:g.894338_894341del	GRCh37
NC_000009.10:g.884338_884341del	NCBI36
NG_009221.1:g.57649_57652del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382276.8:c.822+143_822+146del MANE Select	ENSP00000371711.3:n.822+143_822+146del
ENST00000382276.7:c.822+143_822+146del	ENSP00000371711.3:n.822+143_822+146del
ENST00000564322.1:n.1114_1117del
ENST00000569227.1:c.348+143_348+146del	ENSP00000454701.1:n.348+143_348+146del
NM_021951.2:c.822+143_822+146del	NP_068770.2:n.822+143_822+146del
XM_006716732.1:c.822+143_822+146del	XP_006716795.1:n.822+143_822+146del
XM_011517770.1:c.870+143_870+146del	XP_011516072.1:n.870+143_870+146del
XM_011517771.1:c.870+143_870+146del	XP_011516073.1:n.870+143_870+146del
XM_011517772.1:c.870+143_870+146del	XP_011516074.1:n.870+143_870+146del
XM_011517773.1:c.348+143_348+146del	XP_011516075.1:n.348+143_348+146del
NM_001363767.1:c.348+143_348+146del	NP_001350696.1:n.348+143_348+146del
XM_011517773.3:c.348+143_348+146del	XP_011516075.1:n.348+143_348+146del
XM_017014374.1:c.587-22425_587-22422del	XP_016869863.1:n.587-22425_587-22422del
XM_017014375.1:c.539-22425_539-22422del	XP_016869864.1:n.539-22425_539-22422del
XM_024447434.1:c.276+143_276+146del	XP_024303202.1:n.276+143_276+146del
NM_021951.3:c.822+143_822+146del MANE Select	NP_068770.2:n.822+143_822+146del