Canonical Allele Identifier: CA467208130

Gene: NR5A1

Linked Data

• MyVariant Identifiers: chr9:g.127262813G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.124500534G>C , CM000671.2:g.124500534G>C	GRCh38
NC_000009.11:g.127262813G>C , CM000671.1:g.127262813G>C	GRCh37
NC_000009.10:g.126302634G>C	NCBI36
NG_008176.1:g.11887C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373588.9:c.426C>G MANE Select	ENSP00000362690.4:p.Pro142=
ENST00000373587.3:c.40-262C>G	ENSP00000362689.3:n.40-262C>G
ENST00000373588.8:c.426C>G	ENSP00000362690.4:p.Pro142=
ENST00000455734.1:c.426C>G	ENSP00000393245.1:p.Pro142=
ENST00000620110.4:c.426C>G	ENSP00000483309.1:p.Pro142=
NM_004959.4:c.426C>G	NP_004950.2:p.Pro142=
XM_005251871.2:c.426C>G	XP_005251928.1:p.Pro142=
XM_005251872.3:c.165C>G	XP_005251929.1:p.Pro55=
XM_011518455.1:c.426C>G	XP_011516757.1:p.Pro142=
XM_011518456.1:c.426C>G	XP_011516758.1:p.Pro142=
NM_004959.5:c.426C>G MANE Select	NP_004950.2:p.Pro142=