Canonical Allele Identifier: CA1827191095
Gene: DMRT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.894330_894356delinsACACACATATGTGTGTGTGCCATTTTG , CM000671.2:g.894330_894356delinsACACACATATGTGTGTGTGCCATTTTG GRCh38
NC_000009.11:g.894330_894356delinsACACACATATGTGTGTGTGCCATTTTG , CM000671.1:g.894330_894356delinsACACACATATGTGTGTGTGCCATTTTG GRCh37
NC_000009.10:g.884330_884356delinsACACACATATGTGTGTGTGCCATTTTG NCBI36
NG_009221.1:g.57641_57667delinsACACACATATGTGTGTGTGCCATTTTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000382276.8:c.822+135_822+161delinsACACACATATGTGTGTGTGCCATTTTG MANE Select ENSP00000371711.3:n.822+135_822+161delinsACACACATATGTGTGTGTGC...
ENST00000382276.7:c.822+135_822+161delinsACACACATATGTGTGTGTGCCATTTTG ENSP00000371711.3:n.822+135_822+161delinsACACACATATGTGTGTGTGC...
ENST00000564322.1:n.1106_1132delinsACACACATATGTGTGTGTGCCATTTTG
ENST00000569227.1:c.348+135_348+161delinsACACACATATGTGTGTGTGCCATTTTG ENSP00000454701.1:n.348+135_348+161delinsACACACATATGTGTGTGTGC...
NM_021951.2:c.822+135_822+161delinsACACACATATGTGTGTGTGCCATTTTG NP_068770.2:n.822+135_822+161delinsACACACATATGTGTGTGTGCCATTTT...
XM_006716732.1:c.822+135_822+161delinsACACACATATGTGTGTGTGCCATTTTG XP_006716795.1:n.822+135_822+161delinsACACACATATGTGTGTGTGCCAT...
XM_011517770.1:c.870+135_870+161delinsACACACATATGTGTGTGTGCCATTTTG XP_011516072.1:n.870+135_870+161delinsACACACATATGTGTGTGTGCCAT...
XM_011517771.1:c.870+135_870+161delinsACACACATATGTGTGTGTGCCATTTTG XP_011516073.1:n.870+135_870+161delinsACACACATATGTGTGTGTGCCAT...
XM_011517772.1:c.870+135_870+161delinsACACACATATGTGTGTGTGCCATTTTG XP_011516074.1:n.870+135_870+161delinsACACACATATGTGTGTGTGCCAT...
XM_011517773.1:c.348+135_348+161delinsACACACATATGTGTGTGTGCCATTTTG XP_011516075.1:n.348+135_348+161delinsACACACATATGTGTGTGTGCCAT...
NM_001363767.1:c.348+135_348+161delinsACACACATATGTGTGTGTGCCATTTTG NP_001350696.1:n.348+135_348+161delinsACACACATATGTGTGTGTGCCAT...
XM_011517773.3:c.348+135_348+161delinsACACACATATGTGTGTGTGCCATTTTG XP_011516075.1:n.348+135_348+161delinsACACACATATGTGTGTGTGCCAT...
XM_017014374.1:c.587-22433_587-22407delinsACACACATATGTGTGTGTGCCATTTTG XP_016869863.1:n.587-22433_587-22407delinsACACACATATGTGTGTGTG...
XM_017014375.1:c.539-22433_539-22407delinsACACACATATGTGTGTGTGCCATTTTG XP_016869864.1:n.539-22433_539-22407delinsACACACATATGTGTGTGTG...
XM_024447434.1:c.276+135_276+161delinsACACACATATGTGTGTGTGCCATTTTG XP_024303202.1:n.276+135_276+161delinsACACACATATGTGTGTGTGCCAT...
NM_021951.3:c.822+135_822+161delinsACACACATATGTGTGTGTGCCATTTTG MANE Select NP_068770.2:n.822+135_822+161delinsACACACATATGTGTGTGTGCCATTTT...