Canonical Allele Identifier: CA5235485
Gene: NR5A1 HGNC NCBI

Linked Data

dbSNP Id: rs201340156

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.124500571G>A , CM000671.2:g.124500571G>A GRCh38
NC_000009.11:g.127262850G>A , CM000671.1:g.127262850G>A GRCh37
NC_000009.10:g.126302671G>A NCBI36
NG_008176.1:g.11850C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000373588.9:c.389C>T MANE Select ENSP00000362690.4:p.Pro130Leu
ENST00000373587.3:c.40-299C>T ENSP00000362689.3:n.40-299C>T
ENST00000373588.8:c.389C>T ENSP00000362690.4:p.Pro130Leu
ENST00000455734.1:c.389C>T ENSP00000393245.1:p.Pro130Leu
ENST00000620110.4:c.389C>T ENSP00000483309.1:p.Pro130Leu
NM_004959.4:c.389C>T NP_004950.2:p.Pro130Leu
XM_005251871.2:c.389C>T XP_005251928.1:p.Pro130Leu
XM_005251872.3:c.128C>T XP_005251929.1:p.Pro43Leu
XM_011518455.1:c.389C>T XP_011516757.1:p.Pro130Leu
XM_011518456.1:c.389C>T XP_011516758.1:p.Pro130Leu
NM_004959.5:c.389C>T MANE Select NP_004950.2:p.Pro130Leu