Canonical Allele Identifier: CA1140711949

Gene: NR5A2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.200038802G= , CM000663.2:g.200038802G=	GRCh38
NC_000001.10:g.200007930G= , CM000663.1:g.200007930G=	GRCh37
NC_000001.9:g.198274553G=	NCBI36
NG_050913.1:g.16201G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367362.8:c.65-856G= MANE Select	ENSP00000356331.3:n.65-856G=
ENST00000236914.7:c.65-4972G=	ENSP00000236914.3:n.65-4972G=
ENST00000367362.7:c.65-856G=	ENSP00000356331.3:n.65-856G=
ENST00000447034.1:c.101+30G=
ENST00000474307.1:c.*419-4972G=	ENSP00000436776.1:n.*419-4972G=
NM_003822.4:c.65-4972G=	NP_003813.1:n.65-4972G=
NM_205860.2:c.65-856G=	NP_995582.1:n.65-856G=
XM_011509380.1:c.-56-856G=	XP_011507682.1:n.-56-856G=
XM_011509381.1:c.-57+30G=	XP_011507683.1:n.-57+30G=
XM_011509382.1:c.-14-4972G=	XP_011507684.1:n.-14-4972G=
XM_011509381.3:c.-57+30G=	XP_011507683.1:n.-57+30G=
NM_205860.3:c.65-856G= MANE Select	NP_995582.1:n.65-856G=
NM_003822.5:c.65-4972G=	NP_003813.1:n.65-4972G=