Canonical Allele Identifier: CA1878461899

Gene: NR5A1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.124493016G= , CM000671.2:g.124493016G=	GRCh38
NC_000009.11:g.127255295G= , CM000671.1:g.127255295G=	GRCh37
NC_000009.10:g.126295116G=	NCBI36
NG_008176.1:g.19405C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373588.9:c.990+14C= MANE Select	ENSP00000362690.4:n.990+14C=
ENST00000373587.3:c.342+14C=	ENSP00000362689.3:n.342+14C=
ENST00000373588.8:c.990+14C=	ENSP00000362690.4:n.990+14C=
ENST00000620110.4:c.871-1788C=	ENSP00000483309.1:n.871-1788C=
NM_004959.4:c.990+14C=	NP_004950.2:n.990+14C=
XM_005251871.2:c.990+14C=	XP_005251928.1:n.990+14C=
XM_005251872.3:c.729+14C=	XP_005251929.1:n.729+14C=
XM_011518455.1:c.990+14C=	XP_011516757.1:n.990+14C=
XM_011518456.1:c.870+7074C=	XP_011516758.1:n.870+7074C=
NM_004959.5:c.990+14C= MANE Select	NP_004950.2:n.990+14C=