Canonical Allele Identifier: CA1219157811

Gene: NR5A2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.200038705A= , CM000663.2:g.200038705A=	GRCh38
NC_000001.10:g.200007833A= , CM000663.1:g.200007833A=	GRCh37
NC_000001.9:g.198274456A=	NCBI36
NG_050913.1:g.16104A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367362.8:c.65-953A= MANE Select	ENSP00000356331.3:n.65-953A=
ENST00000236914.7:c.65-5069A=	ENSP00000236914.3:n.65-5069A=
ENST00000367362.7:c.65-953A=	ENSP00000356331.3:n.65-953A=
ENST00000447034.1:c.34A=
ENST00000474307.1:c.*419-5069A=	ENSP00000436776.1:n.*419-5069A=
NM_003822.4:c.65-5069A=	NP_003813.1:n.65-5069A=
NM_205860.2:c.65-953A=	NP_995582.1:n.65-953A=
XM_011509380.1:c.-56-953A=	XP_011507682.1:n.-56-953A=
XM_011509382.1:c.-14-5069A=	XP_011507684.1:n.-14-5069A=
XM_011509381.3:c.-124A=	XP_011507683.1:n.-124A=
NM_205860.3:c.65-953A= MANE Select	NP_995582.1:n.65-953A=
NM_003822.5:c.65-5069A=	NP_003813.1:n.65-5069A=