Canonical Allele Identifier: CA1827191002

Gene: DMRT1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.894271_894297delinsACAGAGGCACACACGCACTTGTGCGCC , CM000671.2:g.894271_894297delinsACAGAGGCACACACGCACTTGTGCGCC	GRCh38
NC_000009.11:g.894271_894297delinsACAGAGGCACACACGCACTTGTGCGCC , CM000671.1:g.894271_894297delinsACAGAGGCACACACGCACTTGTGCGCC	GRCh37
NC_000009.10:g.884271_884297delinsACAGAGGCACACACGCACTTGTGCGCC	NCBI36
NG_009221.1:g.57582_57608delinsACAGAGGCACACACGCACTTGTGCGCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382276.8:c.822+76_822+102delinsACAGAGGCACACACGCACTTGTGCGCC MANE Select	ENSP00000371711.3:n.822+76_822+102delinsACAGAGGCACACACGCACTTG...
ENST00000382276.7:c.822+76_822+102delinsACAGAGGCACACACGCACTTGTGCGCC	ENSP00000371711.3:n.822+76_822+102delinsACAGAGGCACACACGCACTTG...
ENST00000564322.1:n.1047_1073delinsACAGAGGCACACACGCACTTGTGCGCC
ENST00000569227.1:c.348+76_348+102delinsACAGAGGCACACACGCACTTGTGCGCC	ENSP00000454701.1:n.348+76_348+102delinsACAGAGGCACACACGCACTTG...
NM_021951.2:c.822+76_822+102delinsACAGAGGCACACACGCACTTGTGCGCC	NP_068770.2:n.822+76_822+102delinsACAGAGGCACACACGCACTTGTGCGCC...
XM_006716732.1:c.822+76_822+102delinsACAGAGGCACACACGCACTTGTGCGCC	XP_006716795.1:n.822+76_822+102delinsACAGAGGCACACACGCACTTGTGC...
XM_011517770.1:c.870+76_870+102delinsACAGAGGCACACACGCACTTGTGCGCC	XP_011516072.1:n.870+76_870+102delinsACAGAGGCACACACGCACTTGTGC...
XM_011517771.1:c.870+76_870+102delinsACAGAGGCACACACGCACTTGTGCGCC	XP_011516073.1:n.870+76_870+102delinsACAGAGGCACACACGCACTTGTGC...
XM_011517772.1:c.870+76_870+102delinsACAGAGGCACACACGCACTTGTGCGCC	XP_011516074.1:n.870+76_870+102delinsACAGAGGCACACACGCACTTGTGC...
XM_011517773.1:c.348+76_348+102delinsACAGAGGCACACACGCACTTGTGCGCC	XP_011516075.1:n.348+76_348+102delinsACAGAGGCACACACGCACTTGTGC...
NM_001363767.1:c.348+76_348+102delinsACAGAGGCACACACGCACTTGTGCGCC	NP_001350696.1:n.348+76_348+102delinsACAGAGGCACACACGCACTTGTGC...
XM_011517773.3:c.348+76_348+102delinsACAGAGGCACACACGCACTTGTGCGCC	XP_011516075.1:n.348+76_348+102delinsACAGAGGCACACACGCACTTGTGC...
XM_017014374.1:c.587-22492_587-22466delinsACAGAGGCACACACGCACTTGTGCGCC	XP_016869863.1:n.587-22492_587-22466delinsACAGAGGCACACACGCACT...
XM_017014375.1:c.539-22492_539-22466delinsACAGAGGCACACACGCACTTGTGCGCC	XP_016869864.1:n.539-22492_539-22466delinsACAGAGGCACACACGCACT...
XM_024447434.1:c.276+76_276+102delinsACAGAGGCACACACGCACTTGTGCGCC	XP_024303202.1:n.276+76_276+102delinsACAGAGGCACACACGCACTTGTGC...
NM_021951.3:c.822+76_822+102delinsACAGAGGCACACACGCACTTGTGCGCC MANE Select	NP_068770.2:n.822+76_822+102delinsACAGAGGCACACACGCACTTGTGCGCC...