Canonical Allele Identifier: CA1219157559

Gene: NR5A2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.200038172_200038173delinsTG , CM000663.2:g.200038172_200038173delinsTG	GRCh38
NC_000001.10:g.200007300_200007301delinsTG , CM000663.1:g.200007300_200007301delinsTG	GRCh37
NC_000001.9:g.198273923_198273924delinsTG	NCBI36
NG_050913.1:g.15571_15572delinsTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000367362.8:c.65-1486_65-1485delinsTG MANE Select	ENSP00000356331.3:n.65-1486_65-1485delinsTG
ENST00000236914.7:c.65-5602_65-5601delinsTG	ENSP00000236914.3:n.65-5602_65-5601delinsTG
ENST00000367362.7:c.65-1486_65-1485delinsTG	ENSP00000356331.3:n.65-1486_65-1485delinsTG
ENST00000447034.1:c.30-529_30-528delinsTG
ENST00000474307.1:c.*419-5602_*419-5601delinsTG	ENSP00000436776.1:n.*419-5602_*419-5601delinsTG
NM_003822.4:c.65-5602_65-5601delinsTG	NP_003813.1:n.65-5602_65-5601delinsTG
NM_205860.2:c.65-1486_65-1485delinsTG	NP_995582.1:n.65-1486_65-1485delinsTG
XM_011509380.1:c.-56-1486_-56-1485delinsTG	XP_011507682.1:n.-56-1486_-56-1485delinsTG
XM_011509382.1:c.-14-5602_-14-5601delinsTG	XP_011507684.1:n.-14-5602_-14-5601delinsTG
XM_011509381.3:c.-657_-656delinsTG	XP_011507683.1:n.-657_-656delinsTG
NM_205860.3:c.65-1486_65-1485delinsTG MANE Select	NP_995582.1:n.65-1486_65-1485delinsTG
NM_003822.5:c.65-5602_65-5601delinsTG	NP_003813.1:n.65-5602_65-5601delinsTG