Canonical Allele Identifier: CA1827191121

Gene: DMRT1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.894338_894364delinsATGTGTGTGTGCCATTTTGCACACATG , CM000671.2:g.894338_894364delinsATGTGTGTGTGCCATTTTGCACACATG	GRCh38
NC_000009.11:g.894338_894364delinsATGTGTGTGTGCCATTTTGCACACATG , CM000671.1:g.894338_894364delinsATGTGTGTGTGCCATTTTGCACACATG	GRCh37
NC_000009.10:g.884338_884364delinsATGTGTGTGTGCCATTTTGCACACATG	NCBI36
NG_009221.1:g.57649_57675delinsATGTGTGTGTGCCATTTTGCACACATG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382276.8:c.822+143_822+169delinsATGTGTGTGTGCCATTTTGCACACATG MANE Select	ENSP00000371711.3:n.822+143_822+169delinsATGTGTGTGTGCCATTTTGC...
ENST00000382276.7:c.822+143_822+169delinsATGTGTGTGTGCCATTTTGCACACATG	ENSP00000371711.3:n.822+143_822+169delinsATGTGTGTGTGCCATTTTGC...
ENST00000564322.1:n.1114_1140delinsATGTGTGTGTGCCATTTTGCACACATG
ENST00000569227.1:c.348+143_348+169delinsATGTGTGTGTGCCATTTTGCACACATG	ENSP00000454701.1:n.348+143_348+169delinsATGTGTGTGTGCCATTTTGC...
NM_021951.2:c.822+143_822+169delinsATGTGTGTGTGCCATTTTGCACACATG	NP_068770.2:n.822+143_822+169delinsATGTGTGTGTGCCATTTTGCACACAT...
XM_006716732.1:c.822+143_822+169delinsATGTGTGTGTGCCATTTTGCACACATG	XP_006716795.1:n.822+143_822+169delinsATGTGTGTGTGCCATTTTGCACA...
XM_011517770.1:c.870+143_870+169delinsATGTGTGTGTGCCATTTTGCACACATG	XP_011516072.1:n.870+143_870+169delinsATGTGTGTGTGCCATTTTGCACA...
XM_011517771.1:c.870+143_870+169delinsATGTGTGTGTGCCATTTTGCACACATG	XP_011516073.1:n.870+143_870+169delinsATGTGTGTGTGCCATTTTGCACA...
XM_011517772.1:c.870+143_870+169delinsATGTGTGTGTGCCATTTTGCACACATG	XP_011516074.1:n.870+143_870+169delinsATGTGTGTGTGCCATTTTGCACA...
XM_011517773.1:c.348+143_348+169delinsATGTGTGTGTGCCATTTTGCACACATG	XP_011516075.1:n.348+143_348+169delinsATGTGTGTGTGCCATTTTGCACA...
NM_001363767.1:c.348+143_348+169delinsATGTGTGTGTGCCATTTTGCACACATG	NP_001350696.1:n.348+143_348+169delinsATGTGTGTGTGCCATTTTGCACA...
XM_011517773.3:c.348+143_348+169delinsATGTGTGTGTGCCATTTTGCACACATG	XP_011516075.1:n.348+143_348+169delinsATGTGTGTGTGCCATTTTGCACA...
XM_017014374.1:c.587-22425_587-22399delinsATGTGTGTGTGCCATTTTGCACACATG	XP_016869863.1:n.587-22425_587-22399delinsATGTGTGTGTGCCATTTTG...
XM_017014375.1:c.539-22425_539-22399delinsATGTGTGTGTGCCATTTTGCACACATG	XP_016869864.1:n.539-22425_539-22399delinsATGTGTGTGTGCCATTTTG...
XM_024447434.1:c.276+143_276+169delinsATGTGTGTGTGCCATTTTGCACACATG	XP_024303202.1:n.276+143_276+169delinsATGTGTGTGTGCCATTTTGCACA...
NM_021951.3:c.822+143_822+169delinsATGTGTGTGTGCCATTTTGCACACATG MANE Select	NP_068770.2:n.822+143_822+169delinsATGTGTGTGTGCCATTTTGCACACAT...