Canonical Allele Identifier: CA1878470242

Gene: NR5A1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.124500965A= , CM000671.2:g.124500965A=	GRCh38
NC_000009.11:g.127263244A= , CM000671.1:g.127263244A=	GRCh37
NC_000009.10:g.126303065A=	NCBI36
NG_008176.1:g.11456T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373588.9:c.245-250T= MANE Select	ENSP00000362690.4:n.245-250T=
ENST00000373587.3:c.22T=	ENSP00000362689.3:p.Ser8=
ENST00000373588.8:c.245-250T=	ENSP00000362690.4:n.245-250T=
ENST00000455734.1:c.245-250T=	ENSP00000393245.1:n.245-250T=
ENST00000620110.4:c.245-250T=	ENSP00000483309.1:n.245-250T=
NM_004959.4:c.245-250T=	NP_004950.2:n.245-250T=
XM_005251871.2:c.245-250T=	XP_005251928.1:n.245-250T=
XM_005251872.3:c.-17-250T=	XP_005251929.1:n.-17-250T=
XM_011518455.1:c.245-250T=	XP_011516757.1:n.245-250T=
XM_011518456.1:c.245-250T=	XP_011516758.1:n.245-250T=
NM_004959.5:c.245-250T= MANE Select	NP_004950.2:n.245-250T=