Canonical Allele Identifier: CA374887008
Gene: NR5A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.124500448A>T , CM000671.2:g.124500448A>T GRCh38
NC_000009.11:g.127262727A>T , CM000671.1:g.127262727A>T GRCh37
NC_000009.10:g.126302548A>T NCBI36
NG_008176.1:g.11973T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000373588.9:c.512T>A MANE Select ENSP00000362690.4:p.Met171Lys
ENST00000373587.3:c.40-176T>A ENSP00000362689.3:n.40-176T>A
ENST00000373588.8:c.512T>A ENSP00000362690.4:p.Met171Lys
ENST00000455734.1:c.512T>A ENSP00000393245.1:p.Met171Lys
ENST00000620110.4:c.512T>A ENSP00000483309.1:p.Met171Lys
NM_004959.4:c.512T>A NP_004950.2:p.Met171Lys
XM_005251871.2:c.512T>A XP_005251928.1:p.Met171Lys
XM_005251872.3:c.251T>A XP_005251929.1:p.Met84Lys
XM_011518455.1:c.512T>A XP_011516757.1:p.Met171Lys
XM_011518456.1:c.512T>A XP_011516758.1:p.Met171Lys
NM_004959.5:c.512T>A MANE Select NP_004950.2:p.Met171Lys