Canonical Allele Identifier: CA374887665

Gene: NR5A1

Linked Data

• dbSNP Id: rs1322643873
• gnomAD v2: 9-127262770-G-A
• gnomAD v4: 9-124500491-G-A
• MyVariant Identifiers: chr9:g.127262770G>A (hg19) ; chr9:g.127262770_127262779delinsATGGACCGGC (hg19) ; chr9:g.124500491G>A (hg38) ; chr9:g.124500491_124500500delinsATGGACCGGC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.124500491G>A , CM000671.2:g.124500491G>A	GRCh38
NC_000009.11:g.127262770G>A , CM000671.1:g.127262770G>A	GRCh37
NC_000009.10:g.126302591G>A	NCBI36
NG_008176.1:g.11930C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373588.9:c.469C>T MANE Select	ENSP00000362690.4:p.Pro157Ser
ENST00000373587.3:c.40-219C>T	ENSP00000362689.3:n.40-219C>T
ENST00000373588.8:c.469C>T	ENSP00000362690.4:p.Pro157Ser
ENST00000455734.1:c.469C>T	ENSP00000393245.1:p.Pro157Ser
ENST00000620110.4:c.469C>T	ENSP00000483309.1:p.Pro157Ser
NM_004959.4:c.469C>T	NP_004950.2:p.Pro157Ser
XM_005251871.2:c.469C>T	XP_005251928.1:p.Pro157Ser
XM_005251872.3:c.208C>T	XP_005251929.1:p.Pro70Ser
XM_011518455.1:c.469C>T	XP_011516757.1:p.Pro157Ser
XM_011518456.1:c.469C>T	XP_011516758.1:p.Pro157Ser
NM_004959.5:c.469C>T MANE Select	NP_004950.2:p.Pro157Ser