Canonical Allele Identifier: CA2691629861

Gene: NR5A1

Linked Data

• gnomAD v4: 9-124503050-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.124503050T>G , CM000671.2:g.124503050T>G	GRCh38
NC_000009.11:g.127265329T>G , CM000671.1:g.127265329T>G	GRCh37
NC_000009.10:g.126305150T>G	NCBI36
NG_008176.1:g.9371A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373588.9:c.244+29A>C MANE Select	ENSP00000362690.4:n.244+29A>C
ENST00000373588.8:c.244+29A>C	ENSP00000362690.4:n.244+29A>C
ENST00000455734.1:c.244+29A>C	ENSP00000393245.1:n.244+29A>C
ENST00000620110.4:c.244+29A>C	ENSP00000483309.1:n.244+29A>C
NM_004959.4:c.244+29A>C	NP_004950.2:n.244+29A>C
XM_005251871.2:c.244+29A>C	XP_005251928.1:n.244+29A>C
XM_005251872.3:c.-18+244A>C	XP_005251929.1:n.-18+244A>C
XM_011518455.1:c.244+29A>C	XP_011516757.1:n.244+29A>C
XM_011518456.1:c.244+29A>C	XP_011516758.1:n.244+29A>C
NM_004959.5:c.244+29A>C MANE Select	NP_004950.2:n.244+29A>C