Canonical Allele Identifier: CA1219157599

Gene: NR5A2

Linked Data

• dbSNP Id: rs1661874276
• gnomAD v3: 1-200038263-AT-A
• gnomAD v4: 1-200038263-AT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.200038264del , CM000663.2:g.200038264del	GRCh38
NC_000001.10:g.200007392del , CM000663.1:g.200007392del	GRCh37
NC_000001.9:g.198274015del	NCBI36
NG_050913.1:g.15663del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367362.8:c.65-1394del MANE Select	ENSP00000356331.3:n.65-1394del
ENST00000236914.7:c.65-5510del	ENSP00000236914.3:n.65-5510del
ENST00000367362.7:c.65-1394del	ENSP00000356331.3:n.65-1394del
ENST00000447034.1:c.30-437del
ENST00000474307.1:c.*419-5510del	ENSP00000436776.1:n.*419-5510del
NM_003822.4:c.65-5510del	NP_003813.1:n.65-5510del
NM_205860.2:c.65-1394del	NP_995582.1:n.65-1394del
XM_011509380.1:c.-56-1394del	XP_011507682.1:n.-56-1394del
XM_011509382.1:c.-14-5510del	XP_011507684.1:n.-14-5510del
XM_011509381.3:c.-565del	XP_011507683.1:n.-565del
NM_205860.3:c.65-1394del MANE Select	NP_995582.1:n.65-1394del
NM_003822.5:c.65-5510del	NP_003813.1:n.65-5510del