Canonical Allele Identifier: CA1219157547
Gene: NR5A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.200038149_200038151delinsGGT , CM000663.2:g.200038149_200038151delinsGGT GRCh38
NC_000001.10:g.200007277_200007279delinsGGT , CM000663.1:g.200007277_200007279delinsGGT GRCh37
NC_000001.9:g.198273900_198273902delinsGGT NCBI36
NG_050913.1:g.15548_15550delinsGGT

Transcript Alleles

HGVS Amino-acid change
ENST00000367362.8:c.65-1509_65-1507delinsGGT MANE Select ENSP00000356331.3:n.65-1509_65-1507delins...
ENST00000236914.7:c.65-5625_65-5623delinsGGT ENSP00000236914.3:n.65-5625_65-5623delins...
ENST00000367362.7:c.65-1509_65-1507delinsGGT ENSP00000356331.3:n.65-1509_65-1507delins...
ENST00000447034.1:c.30-552_30-550delinsGGT
ENST00000474307.1:c.*419-5625_*419-5623delinsGGT ENSP00000436776.1:n.*419-5625_*419-5623de...
NM_003822.4:c.65-5625_65-5623delinsGGT NP_003813.1:n.65-5625_65-5623delinsGGT
NM_205860.2:c.65-1509_65-1507delinsGGT NP_995582.1:n.65-1509_65-1507delinsGGT
XM_011509380.1:c.-56-1509_-56-1507delinsGGT XP_011507682.1:n.-56-1509_-56-1507delinsG...
XM_011509382.1:c.-14-5625_-14-5623delinsGGT XP_011507684.1:n.-14-5625_-14-5623delinsG...
XM_011509381.3:c.-680_-678delinsGGT XP_011507683.1:n.-680_-678delinsGGT
NM_205860.3:c.65-1509_65-1507delinsGGT MANE Select NP_995582.1:n.65-1509_65-1507delinsGGT
NM_003822.5:c.65-5625_65-5623delinsGGT NP_003813.1:n.65-5625_65-5623delinsGGT