Canonical Allele Identifier: CA374887497
Gene: NR5A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.124500472T>G , CM000671.2:g.124500472T>G GRCh38
NC_000009.11:g.127262751T>G , CM000671.1:g.127262751T>G GRCh37
NC_000009.10:g.126302572T>G NCBI36
NG_008176.1:g.11949A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000373588.9:c.488A>C MANE Select ENSP00000362690.4:p.Asp163Ala
ENST00000373587.3:c.40-200A>C ENSP00000362689.3:n.40-200A>C
ENST00000373588.8:c.488A>C ENSP00000362690.4:p.Asp163Ala
ENST00000455734.1:c.488A>C ENSP00000393245.1:p.Asp163Ala
ENST00000620110.4:c.488A>C ENSP00000483309.1:p.Asp163Ala
NM_004959.4:c.488A>C NP_004950.2:p.Asp163Ala
XM_005251871.2:c.488A>C XP_005251928.1:p.Asp163Ala
XM_005251872.3:c.227A>C XP_005251929.1:p.Asp76Ala
XM_011518455.1:c.488A>C XP_011516757.1:p.Asp163Ala
XM_011518456.1:c.488A>C XP_011516758.1:p.Asp163Ala
NM_004959.5:c.488A>C MANE Select NP_004950.2:p.Asp163Ala