Canonical Allele Identifier: CA1878470311

Gene: NR5A1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.124501001T= , CM000671.2:g.124501001T=	GRCh38
NC_000009.11:g.127263280T= , CM000671.1:g.127263280T=	GRCh37
NC_000009.10:g.126303101T=	NCBI36
NG_008176.1:g.11420A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373588.9:c.245-286A= MANE Select	ENSP00000362690.4:n.245-286A=
ENST00000373588.8:c.245-286A=	ENSP00000362690.4:n.245-286A=
ENST00000455734.1:c.245-286A=	ENSP00000393245.1:n.245-286A=
ENST00000620110.4:c.245-286A=	ENSP00000483309.1:n.245-286A=
NM_004959.4:c.245-286A=	NP_004950.2:n.245-286A=
XM_005251871.2:c.245-286A=	XP_005251928.1:n.245-286A=
XM_005251872.3:c.-17-286A=	XP_005251929.1:n.-17-286A=
XM_011518455.1:c.245-286A=	XP_011516757.1:n.245-286A=
XM_011518456.1:c.245-286A=	XP_011516758.1:n.245-286A=
NM_004959.5:c.245-286A= MANE Select	NP_004950.2:n.245-286A=