Canonical Allele Identifier: CA467208165

Gene: NR5A1

Linked Data

• MyVariant Identifiers: chr9:g.127262846C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.124500567C>G , CM000671.2:g.124500567C>G	GRCh38
NC_000009.11:g.127262846C>G , CM000671.1:g.127262846C>G	GRCh37
NC_000009.10:g.126302667C>G	NCBI36
NG_008176.1:g.11854G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373588.9:c.393G>C MANE Select	ENSP00000362690.4:p.Pro131=
ENST00000373587.3:c.40-295G>C	ENSP00000362689.3:n.40-295G>C
ENST00000373588.8:c.393G>C	ENSP00000362690.4:p.Pro131=
ENST00000455734.1:c.393G>C	ENSP00000393245.1:p.Pro131=
ENST00000620110.4:c.393G>C	ENSP00000483309.1:p.Pro131=
NM_004959.4:c.393G>C	NP_004950.2:p.Pro131=
XM_005251871.2:c.393G>C	XP_005251928.1:p.Pro131=
XM_005251872.3:c.132G>C	XP_005251929.1:p.Pro44=
XM_011518455.1:c.393G>C	XP_011516757.1:p.Pro131=
XM_011518456.1:c.393G>C	XP_011516758.1:p.Pro131=
NM_004959.5:c.393G>C MANE Select	NP_004950.2:p.Pro131=