Canonical Allele Identifier: CA1120451164

Gene: DMRT1

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.863635C>A , CM000671.2:g.863635C>A	GRCh38
NC_000009.11:g.863635C>A , CM000671.1:g.863635C>A	GRCh37
NC_000009.10:g.853635C>A	NCBI36
NG_009221.1:g.26946C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382276.8:c.538+16492C>A MANE Select	ENSP00000371711.3:n.538+16492C>A
ENST00000382276.7:c.538+16492C>A	ENSP00000371711.3:n.538+16492C>A
ENST00000564322.1:n.687+16492C>A
ENST00000569227.1:c.64+16492C>A	ENSP00000454701.1:n.64+16492C>A
NM_021951.2:c.538+16492C>A	NP_068770.2:n.538+16492C>A
XM_006716732.1:c.538+16492C>A	XP_006716795.1:n.538+16492C>A
XM_011517770.1:c.586+16492C>A	XP_011516072.1:n.586+16492C>A
XM_011517771.1:c.586+16492C>A	XP_011516073.1:n.586+16492C>A
XM_011517772.1:c.586+16492C>A	XP_011516074.1:n.586+16492C>A
XM_011517773.1:c.64+16492C>A	XP_011516075.1:n.64+16492C>A
NM_001363767.1:c.64+16492C>A	NP_001350696.1:n.64+16492C>A
XM_011517773.3:c.64+16492C>A	XP_011516075.1:n.64+16492C>A
XM_017014374.1:c.586+16492C>A	XP_016869863.1:n.586+16492C>A
XM_017014375.1:c.538+16492C>A	XP_016869864.1:n.538+16492C>A
XM_024447434.1:c.-9+5167C>A	XP_024303202.1:n.-9+5167C>A
NM_021951.3:c.538+16492C>A MANE Select	NP_068770.2:n.538+16492C>A