Canonical Allele Identifier: CA1827156141
Gene: DMRT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.845516A= , CM000671.2:g.845516A= GRCh38
NC_000009.11:g.845516A= , CM000671.1:g.845516A= GRCh37
NC_000009.10:g.835516A= NCBI36
NG_009221.1:g.8827A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000382276.8:c.355-1444A= MANE Select ENSP00000371711.3:n.355-1444A=
ENST00000382276.7:c.355-1444A= ENSP00000371711.3:n.355-1444A=
ENST00000564322.1:n.504-1444A=
ENST00000569227.1:c.-120-1444A= ENSP00000454701.1:n.-120-1444A=
NM_021951.2:c.355-1444A= NP_068770.2:n.355-1444A=
XM_006716732.1:c.355-1444A= XP_006716795.1:n.355-1444A=
XM_011517770.1:c.403-1444A= XP_011516072.1:n.403-1444A=
XM_011517771.1:c.403-1444A= XP_011516073.1:n.403-1444A=
XM_011517772.1:c.403-1444A= XP_011516074.1:n.403-1444A=
XM_011517773.1:c.-120-1444A= XP_011516075.1:n.-120-1444A=
NM_001363767.1:c.-120-1444A= NP_001350696.1:n.-120-1444A=
XM_011517773.3:c.-120-1444A= XP_011516075.1:n.-120-1444A=
XM_017014374.1:c.403-1444A= XP_016869863.1:n.403-1444A=
XM_017014375.1:c.355-1444A= XP_016869864.1:n.355-1444A=
NM_021951.3:c.355-1444A= MANE Select NP_068770.2:n.355-1444A=