Canonical Allele Identifier: CA1219192208

Gene: NR5A2

Linked Data

• dbSNP Id: rs1666458489

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.200121020_200121024dup , CM000663.2:g.200121020_200121024dup	GRCh38
NC_000001.10:g.200090148_200090152dup , CM000663.1:g.200090148_200090152dup	GRCh37
NC_000001.9:g.198356771_198356775dup	NCBI36
NG_050913.1:g.98419_98423dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367362.8:c.1378+65_1378+69dup MANE Select	ENSP00000356331.3:n.1378+65_1378+69dup
ENST00000236914.7:c.1240+65_1240+69dup	ENSP00000236914.3:n.1240+65_1240+69dup
ENST00000367362.7:c.1378+65_1378+69dup	ENSP00000356331.3:n.1378+65_1378+69dup
ENST00000544748.5:c.1162+65_1162+69dup	ENSP00000439116.1:n.1162+65_1162+69dup
NM_001276464.1:c.1162+65_1162+69dup	NP_001263393.1:n.1162+65_1162+69dup
NM_003822.4:c.1240+65_1240+69dup	NP_003813.1:n.1240+65_1240+69dup
NM_205860.2:c.1378+65_1378+69dup	NP_995582.1:n.1378+65_1378+69dup
XM_005245062.2:c.1162+65_1162+69dup	XP_005245119.1:n.1162+65_1162+69dup
XM_011509380.1:c.1258+65_1258+69dup	XP_011507682.1:n.1258+65_1258+69dup
XM_011509381.1:c.1258+65_1258+69dup	XP_011507683.1:n.1258+65_1258+69dup
XM_011509382.1:c.1162+65_1162+69dup	XP_011507684.1:n.1162+65_1162+69dup
XM_011509383.1:c.1162+65_1162+69dup	XP_011507685.1:n.1162+65_1162+69dup
XM_011509384.1:c.1258+65_1258+69dup	XP_011507686.1:n.1258+65_1258+69dup
XM_005245062.3:c.1162+65_1162+69dup	XP_005245119.1:n.1162+65_1162+69dup
XM_011509381.3:c.1258+65_1258+69dup	XP_011507683.1:n.1258+65_1258+69dup
XM_011509384.2:c.1258+65_1258+69dup	XP_011507686.1:n.1258+65_1258+69dup
XM_017000904.1:c.1258+65_1258+69dup	XP_016856393.1:n.1258+65_1258+69dup
NM_205860.3:c.1378+65_1378+69dup MANE Select	NP_995582.1:n.1378+65_1378+69dup
NM_003822.5:c.1240+65_1240+69dup	NP_003813.1:n.1240+65_1240+69dup
NM_001276464.2:c.1162+65_1162+69dup	NP_001263393.1:n.1162+65_1162+69dup