Canonical Allele Identifier: CA1219157628

Gene: NR5A2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.200038324T= , CM000663.2:g.200038324T=	GRCh38
NC_000001.10:g.200007452T= , CM000663.1:g.200007452T=	GRCh37
NC_000001.9:g.198274075T=	NCBI36
NG_050913.1:g.15723T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000367362.8:c.65-1334T= MANE Select	ENSP00000356331.3:n.65-1334T=
ENST00000236914.7:c.65-5450T=	ENSP00000236914.3:n.65-5450T=
ENST00000367362.7:c.65-1334T=	ENSP00000356331.3:n.65-1334T=
ENST00000447034.1:c.30-377T=
ENST00000474307.1:c.*419-5450T=	ENSP00000436776.1:n.*419-5450T=
NM_003822.4:c.65-5450T=	NP_003813.1:n.65-5450T=
NM_205860.2:c.65-1334T=	NP_995582.1:n.65-1334T=
XM_011509380.1:c.-56-1334T=	XP_011507682.1:n.-56-1334T=
XM_011509382.1:c.-14-5450T=	XP_011507684.1:n.-14-5450T=
XM_011509381.3:c.-505T=	XP_011507683.1:n.-505T=
NM_205860.3:c.65-1334T= MANE Select	NP_995582.1:n.65-1334T=
NM_003822.5:c.65-5450T=	NP_003813.1:n.65-5450T=