Canonical Allele Identifier: CA467208264

Gene: NR5A1

Linked Data

• MyVariant Identifiers: chr9:g.127262938G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.124500659G>T , CM000671.2:g.124500659G>T	GRCh38
NC_000009.11:g.127262938G>T , CM000671.1:g.127262938G>T	GRCh37
NC_000009.10:g.126302759G>T	NCBI36
NG_008176.1:g.11762C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373588.9:c.301C>A MANE Select	ENSP00000362690.4:p.Arg101=
ENST00000373587.3:c.39+289C>A	ENSP00000362689.3:n.39+289C>A
ENST00000373588.8:c.301C>A	ENSP00000362690.4:p.Arg101=
ENST00000455734.1:c.301C>A	ENSP00000393245.1:p.Arg101=
ENST00000620110.4:c.301C>A	ENSP00000483309.1:p.Arg101=
NM_004959.4:c.301C>A	NP_004950.2:p.Arg101=
XM_005251871.2:c.301C>A	XP_005251928.1:p.Arg101=
XM_005251872.3:c.40C>A	XP_005251929.1:p.Arg14=
XM_011518455.1:c.301C>A	XP_011516757.1:p.Arg101=
XM_011518456.1:c.301C>A	XP_011516758.1:p.Arg101=
NM_004959.5:c.301C>A MANE Select	NP_004950.2:p.Arg101=