Canonical Allele Identifier: CA1354510836

Gene: RBMS3

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.29913111_29913113delinsACT , CM000665.2:g.29913111_29913113delinsACT	GRCh38
NC_000003.11:g.29954602_29954604delinsACT , CM000665.1:g.29954602_29954604delinsACT	GRCh37
NC_000003.10:g.29929606_29929608delinsACT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000383767.7:c.939+13356_939+13358delinsACT MANE Select	ENSP00000373277.2:n.939+13356_939+13358delinsACT
ENST00000636680.2:c.1317+13356_1317+13358delinsACT	ENSP00000490271.2:n.1317+13356_1317+13358delinsACT
ENST00000637842.1:c.1186+13356_1186+13358delinsACT	ENSP00000489718.1:n.1186+13356_1186+13358delinsACT
ENST00000273139.13:c.939+13356_939+13358delinsACT	ENSP00000273139.9:n.939+13356_939+13358delinsACT
ENST00000383766.6:c.885+15636_885+15638delinsACT	ENSP00000373276.2:n.885+15636_885+15638delinsACT
ENST00000383767.6:c.939+13356_939+13358delinsACT	ENSP00000373277.2:n.939+13356_939+13358delinsACT
ENST00000434693.6:c.936+13356_936+13358delinsACT	ENSP00000395592.1:n.936+13356_936+13358delinsACT
ENST00000452462.5:c.939+13356_939+13358delinsACT	ENSP00000397926.1:n.939+13356_939+13358delinsACT
ENST00000456853.1:c.978+13356_978+13358delinsACT	ENSP00000400519.1:n.978+13356_978+13358delinsACT
NM_001003792.2:c.885+15636_885+15638delinsACT	NP_001003792.1:n.885+15636_885+15638delinsACT
NM_001003793.2:c.939+13356_939+13358delinsACT	NP_001003793.1:n.939+13356_939+13358delinsACT
NM_001177711.1:c.939+13356_939+13358delinsACT	NP_001171182.1:n.939+13356_939+13358delinsACT
NM_001177712.1:c.978+13356_978+13358delinsACT	NP_001171183.1:n.978+13356_978+13358delinsACT
NM_014483.3:c.939+13356_939+13358delinsACT	NP_055298.2:n.939+13356_939+13358delinsACT
XM_005265060.1:c.936+13356_936+13358delinsACT	XP_005265117.1:n.936+13356_936+13358delinsACT
XM_005265061.1:c.888+15636_888+15638delinsACT	XP_005265118.1:n.888+15636_888+15638delinsACT
XM_005265062.1:c.888+15636_888+15638delinsACT	XP_005265119.1:n.888+15636_888+15638delinsACT
XM_005265063.1:c.654+13356_654+13358delinsACT	XP_005265120.1:n.654+13356_654+13358delinsACT
XM_005265064.3:c.654+13356_654+13358delinsACT	XP_005265121.1:n.654+13356_654+13358delinsACT
XM_005265065.3:c.612+13356_612+13358delinsACT	XP_005265122.1:n.612+13356_612+13358delinsACT
XM_011533592.1:c.939+13356_939+13358delinsACT	XP_011531894.1:n.939+13356_939+13358delinsACT
XM_011533593.1:c.939+13356_939+13358delinsACT	XP_011531895.1:n.939+13356_939+13358delinsACT
XM_011533594.1:c.940-11186_940-11184delinsACT	XP_011531896.1:n.940-11186_940-11184delinsACT
NM_001330696.1:c.936+13356_936+13358delinsACT	NP_001317625.1:n.936+13356_936+13358delinsACT
XM_005265061.2:c.888+15636_888+15638delinsACT	XP_005265118.1:n.888+15636_888+15638delinsACT
XM_005265063.2:c.654+13356_654+13358delinsACT	XP_005265120.1:n.654+13356_654+13358delinsACT
XM_005265065.5:c.612+13356_612+13358delinsACT	XP_005265122.1:n.612+13356_612+13358delinsACT
XM_017006178.1:c.936+13356_936+13358delinsACT	XP_016861667.1:n.936+13356_936+13358delinsACT
XM_017006179.1:c.936+13356_936+13358delinsACT	XP_016861668.1:n.936+13356_936+13358delinsACT
XM_017006180.1:c.888+15636_888+15638delinsACT	XP_016861669.1:n.888+15636_888+15638delinsACT
XM_017006181.1:c.885+15636_885+15638delinsACT	XP_016861670.1:n.885+15636_885+15638delinsACT
XM_017006182.1:c.786+15636_786+15638delinsACT	XP_016861671.1:n.786+15636_786+15638delinsACT
XM_024453454.1:c.939+13356_939+13358delinsACT	XP_024309222.1:n.939+13356_939+13358delinsACT
NM_001003792.3:c.885+15636_885+15638delinsACT	NP_001003792.1:n.885+15636_885+15638delinsACT
NM_001003793.3:c.939+13356_939+13358delinsACT MANE Select	NP_001003793.1:n.939+13356_939+13358delinsACT
NM_001177711.2:c.939+13356_939+13358delinsACT	NP_001171182.1:n.939+13356_939+13358delinsACT
NM_001177712.2:c.978+13356_978+13358delinsACT	NP_001171183.1:n.978+13356_978+13358delinsACT
NM_014483.4:c.939+13356_939+13358delinsACT	NP_055298.2:n.939+13356_939+13358delinsACT