Canonical Allele Identifier: CA2842889851
Gene: NR5A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.124500638dup , CM000671.2:g.124500638dup GRCh38
NC_000009.11:g.127262917dup , CM000671.1:g.127262917dup GRCh37
NC_000009.10:g.126302738dup NCBI36
NG_008176.1:g.11783dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000373588.9:c.322dup MANE Select ENSP00000362690.4:p.Gln108ProfsTer?
ENST00000373587.3:c.39+310dup ENSP00000362689.3:n.39+310dup
ENST00000373588.8:c.322dup ENSP00000362690.4:p.Gln108ProfsTer?
ENST00000455734.1:c.322dup ENSP00000393245.1:p.Gln108ProfsTer?
ENST00000620110.4:c.322dup ENSP00000483309.1:p.Gln108ProfsTer?
NM_004959.4:c.322dup NP_004950.2:p.Gln108ProfsTer?
XM_005251871.2:c.322dup XP_005251928.1:p.Gln108ProfsTer?
XM_005251872.3:c.61dup XP_005251929.1:p.Gln21ProfsTer?
XM_011518455.1:c.322dup XP_011516757.1:p.Gln108ProfsTer?
XM_011518456.1:c.322dup XP_011516758.1:p.Gln108ProfsTer?
NM_004959.5:c.322dup MANE Select NP_004950.2:p.Gln108ProfsTer?