Canonical Allele Identifier: CA1146876819

Gene: NR5A2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.200038554C= , CM000663.2:g.200038554C=	GRCh38
NC_000001.10:g.200007682C= , CM000663.1:g.200007682C=	GRCh37
NC_000001.9:g.198274305C=	NCBI36
NG_050913.1:g.15953C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367362.8:c.65-1104C= MANE Select	ENSP00000356331.3:n.65-1104C=
ENST00000236914.7:c.65-5220C=	ENSP00000236914.3:n.65-5220C=
ENST00000367362.7:c.65-1104C=	ENSP00000356331.3:n.65-1104C=
ENST00000447034.1:c.30-147C=
ENST00000474307.1:c.*419-5220C=	ENSP00000436776.1:n.*419-5220C=
NM_003822.4:c.65-5220C=	NP_003813.1:n.65-5220C=
NM_205860.2:c.65-1104C=	NP_995582.1:n.65-1104C=
XM_011509380.1:c.-56-1104C=	XP_011507682.1:n.-56-1104C=
XM_011509382.1:c.-14-5220C=	XP_011507684.1:n.-14-5220C=
XM_011509381.3:c.-275C=	XP_011507683.1:n.-275C=
NM_205860.3:c.65-1104C= MANE Select	NP_995582.1:n.65-1104C=
NM_003822.5:c.65-5220C=	NP_003813.1:n.65-5220C=