Canonical Allele Identifier: CA467121318

Gene: NR5A1

Linked Data

• MyVariant Identifiers: chr9:g.127255381C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.124493102C>A , CM000671.2:g.124493102C>A	GRCh38
NC_000009.11:g.127255381C>A , CM000671.1:g.127255381C>A	GRCh37
NC_000009.10:g.126295202C>A	NCBI36
NG_008176.1:g.19319G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373588.9:c.918G>T MANE Select	ENSP00000362690.4:p.Leu306=
ENST00000373587.3:c.270G>T	ENSP00000362689.3:p.Leu90=
ENST00000373588.8:c.918G>T	ENSP00000362690.4:p.Leu306=
ENST00000620110.4:c.871-1874G>T	ENSP00000483309.1:n.871-1874G>T
NM_004959.4:c.918G>T	NP_004950.2:p.Leu306=
XM_005251871.2:c.918G>T	XP_005251928.1:p.Leu306=
XM_005251872.3:c.657G>T	XP_005251929.1:p.Leu219=
XM_011518455.1:c.918G>T	XP_011516757.1:p.Leu306=
XM_011518456.1:c.870+6988G>T	XP_011516758.1:n.870+6988G>T
NM_004959.5:c.918G>T MANE Select	NP_004950.2:p.Leu306=