Canonical Allele Identifier: CA187851799

Gene: DMRT1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.917015T>G , CM000671.2:g.917015T>G	GRCh38
NC_000009.11:g.917015T>G , CM000671.1:g.917015T>G	GRCh37
NC_000009.10:g.907015T>G	NCBI36
NG_009221.1:g.80326T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_021951.3:c.967+108T>G MANE Select	NP_068770.2:n.967+108T>G
ENST00000382276.8:c.967+108T>G MANE Select	ENSP00000371711.3:n.967+108T>G
NM_001363767.1:c.493+108T>G	NP_001350696.1:n.493+108T>G
NM_021951.2:c.967+108T>G	NP_068770.2:n.967+108T>G
ENST00000382276.7:c.967+108T>G	ENSP00000371711.3:n.967+108T>G
ENST00000569227.1:c.493+108T>G	ENSP00000454701.1:n.493+108T>G
XM_006716732.1:c.970+108T>G	XP_006716795.1:n.970+108T>G
XM_011517770.1:c.1018+108T>G	XP_011516072.1:n.1018+108T>G
XM_011517771.1:c.1015+108T>G	XP_011516073.1:n.1015+108T>G
XM_011517772.1:c.870+22820T>G	XP_011516074.1:n.870+22820T>G
XM_011517773.1:c.496+108T>G	XP_011516075.1:n.496+108T>G
XM_011517773.3:c.496+108T>G	XP_011516075.1:n.496+108T>G
XM_017014374.1:c.*35+108T>G	XP_016869863.1:n.*35+108T>G
XM_017014375.1:c.*35+108T>G	XP_016869864.1:n.*35+108T>G
XM_024447434.1:c.421+108T>G	XP_024303202.1:n.421+108T>G