Canonical Allele Identifier: CA1878469039

Gene: NR5A1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.124500483C= , CM000671.2:g.124500483C=	GRCh38
NC_000009.11:g.127262762C= , CM000671.1:g.127262762C=	GRCh37
NC_000009.10:g.126302583C=	NCBI36
NG_008176.1:g.11938G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000373588.9:c.477G= MANE Select	ENSP00000362690.4:p.Gly159=
ENST00000373587.3:c.40-211G=	ENSP00000362689.3:n.40-211G=
ENST00000373588.8:c.477G=	ENSP00000362690.4:p.Gly159=
ENST00000455734.1:c.477G=	ENSP00000393245.1:p.Gly159=
ENST00000620110.4:c.477G=	ENSP00000483309.1:p.Gly159=
NM_004959.4:c.477G=	NP_004950.2:p.Gly159=
XM_005251871.2:c.477G=	XP_005251928.1:p.Gly159=
XM_005251872.3:c.216G=	XP_005251929.1:p.Gly72=
XM_011518455.1:c.477G=	XP_011516757.1:p.Gly159=
XM_011518456.1:c.477G=	XP_011516758.1:p.Gly159=
NM_004959.5:c.477G= MANE Select	NP_004950.2:p.Gly159=