Canonical Allele Identifier: CA374882493
Gene: NR5A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.124493112C>G , CM000671.2:g.124493112C>G GRCh38
NC_000009.11:g.127255391C>G , CM000671.1:g.127255391C>G GRCh37
NC_000009.10:g.126295212C>G NCBI36
NG_008176.1:g.19309G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000373588.9:c.908G>C MANE Select ENSP00000362690.4:p.Ser303Thr
ENST00000373587.3:c.260G>C ENSP00000362689.3:p.Ser87Thr
ENST00000373588.8:c.908G>C ENSP00000362690.4:p.Ser303Thr
ENST00000620110.4:c.871-1884G>C ENSP00000483309.1:n.871-1884G>C
NM_004959.4:c.908G>C NP_004950.2:p.Ser303Thr
XM_005251871.2:c.908G>C XP_005251928.1:p.Ser303Thr
XM_005251872.3:c.647G>C XP_005251929.1:p.Ser216Thr
XM_011518455.1:c.908G>C XP_011516757.1:p.Ser303Thr
XM_011518456.1:c.870+6978G>C XP_011516758.1:n.870+6978G>C
NM_004959.5:c.908G>C MANE Select NP_004950.2:p.Ser303Thr