Canonical Allele Identifier: CA1878468222

Gene: NR5A1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.124500196C= , CM000671.2:g.124500196C=	GRCh38
NC_000009.11:g.127262475C= , CM000671.1:g.127262475C=	GRCh37
NC_000009.10:g.126302296C=	NCBI36
NG_008176.1:g.12225G=

Transcript Alleles

HGVS	Amino-acid Change
NM_004959.5:c.764G= MANE Select	NP_004950.2:p.Arg255=
ENST00000373588.9:c.764G= MANE Select	ENSP00000362690.4:p.Arg255=
NM_004959.4:c.764G=	NP_004950.2:p.Arg255=
ENST00000373587.3:c.116G=	ENSP00000362689.3:p.Arg39=
ENST00000373588.8:c.764G=	ENSP00000362690.4:p.Arg255=
ENST00000620110.4:c.764G=	ENSP00000483309.1:p.Arg255=
XM_005251871.2:c.764G=	XP_005251928.1:p.Arg255=
XM_005251872.3:c.503G=	XP_005251929.1:p.Arg168=
XM_011518455.1:c.764G=	XP_011516757.1:p.Arg255=
XM_011518456.1:c.764G=	XP_011516758.1:p.Arg255=