Canonical Allele Identifier: CA1354510862

Gene: RBMS3

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.29913172_29913173delinsCT , CM000665.2:g.29913172_29913173delinsCT	GRCh38
NC_000003.11:g.29954663_29954664delinsCT , CM000665.1:g.29954663_29954664delinsCT	GRCh37
NC_000003.10:g.29929667_29929668delinsCT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000383767.7:c.939+13417_939+13418delinsCT MANE Select	ENSP00000373277.2:n.939+13417_939+13418delinsCT
ENST00000636680.2:c.1317+13417_1317+13418delinsCT	ENSP00000490271.2:n.1317+13417_1317+13418delinsCT
ENST00000637842.1:c.1186+13417_1186+13418delinsCT	ENSP00000489718.1:n.1186+13417_1186+13418delinsCT
ENST00000273139.13:c.939+13417_939+13418delinsCT	ENSP00000273139.9:n.939+13417_939+13418delinsCT
ENST00000383766.6:c.885+15697_885+15698delinsCT	ENSP00000373276.2:n.885+15697_885+15698delinsCT
ENST00000383767.6:c.939+13417_939+13418delinsCT	ENSP00000373277.2:n.939+13417_939+13418delinsCT
ENST00000434693.6:c.936+13417_936+13418delinsCT	ENSP00000395592.1:n.936+13417_936+13418delinsCT
ENST00000452462.5:c.939+13417_939+13418delinsCT	ENSP00000397926.1:n.939+13417_939+13418delinsCT
ENST00000456853.1:c.978+13417_978+13418delinsCT	ENSP00000400519.1:n.978+13417_978+13418delinsCT
NM_001003792.2:c.885+15697_885+15698delinsCT	NP_001003792.1:n.885+15697_885+15698delinsCT
NM_001003793.2:c.939+13417_939+13418delinsCT	NP_001003793.1:n.939+13417_939+13418delinsCT
NM_001177711.1:c.939+13417_939+13418delinsCT	NP_001171182.1:n.939+13417_939+13418delinsCT
NM_001177712.1:c.978+13417_978+13418delinsCT	NP_001171183.1:n.978+13417_978+13418delinsCT
NM_014483.3:c.939+13417_939+13418delinsCT	NP_055298.2:n.939+13417_939+13418delinsCT
XM_005265060.1:c.936+13417_936+13418delinsCT	XP_005265117.1:n.936+13417_936+13418delinsCT
XM_005265061.1:c.888+15697_888+15698delinsCT	XP_005265118.1:n.888+15697_888+15698delinsCT
XM_005265062.1:c.888+15697_888+15698delinsCT	XP_005265119.1:n.888+15697_888+15698delinsCT
XM_005265063.1:c.654+13417_654+13418delinsCT	XP_005265120.1:n.654+13417_654+13418delinsCT
XM_005265064.3:c.654+13417_654+13418delinsCT	XP_005265121.1:n.654+13417_654+13418delinsCT
XM_005265065.3:c.612+13417_612+13418delinsCT	XP_005265122.1:n.612+13417_612+13418delinsCT
XM_011533592.1:c.939+13417_939+13418delinsCT	XP_011531894.1:n.939+13417_939+13418delinsCT
XM_011533593.1:c.939+13417_939+13418delinsCT	XP_011531895.1:n.939+13417_939+13418delinsCT
XM_011533594.1:c.940-11125_940-11124delinsCT	XP_011531896.1:n.940-11125_940-11124delinsCT
NM_001330696.1:c.936+13417_936+13418delinsCT	NP_001317625.1:n.936+13417_936+13418delinsCT
XM_005265061.2:c.888+15697_888+15698delinsCT	XP_005265118.1:n.888+15697_888+15698delinsCT
XM_005265063.2:c.654+13417_654+13418delinsCT	XP_005265120.1:n.654+13417_654+13418delinsCT
XM_005265065.5:c.612+13417_612+13418delinsCT	XP_005265122.1:n.612+13417_612+13418delinsCT
XM_017006178.1:c.936+13417_936+13418delinsCT	XP_016861667.1:n.936+13417_936+13418delinsCT
XM_017006179.1:c.936+13417_936+13418delinsCT	XP_016861668.1:n.936+13417_936+13418delinsCT
XM_017006180.1:c.888+15697_888+15698delinsCT	XP_016861669.1:n.888+15697_888+15698delinsCT
XM_017006181.1:c.885+15697_885+15698delinsCT	XP_016861670.1:n.885+15697_885+15698delinsCT
XM_017006182.1:c.786+15697_786+15698delinsCT	XP_016861671.1:n.786+15697_786+15698delinsCT
XM_024453454.1:c.939+13417_939+13418delinsCT	XP_024309222.1:n.939+13417_939+13418delinsCT
NM_001003792.3:c.885+15697_885+15698delinsCT	NP_001003792.1:n.885+15697_885+15698delinsCT
NM_001003793.3:c.939+13417_939+13418delinsCT MANE Select	NP_001003793.1:n.939+13417_939+13418delinsCT
NM_001177711.2:c.939+13417_939+13418delinsCT	NP_001171182.1:n.939+13417_939+13418delinsCT
NM_001177712.2:c.978+13417_978+13418delinsCT	NP_001171183.1:n.978+13417_978+13418delinsCT
NM_014483.4:c.939+13417_939+13418delinsCT	NP_055298.2:n.939+13417_939+13418delinsCT