Canonical Allele Identifier: CA471507071

Gene: RBM20

Linked Data

• COSMIC: COSM1345775
• MyVariant Identifiers: chr10:g.112572540del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.110812786del , CM000672.2:g.110812786del	GRCh38
NC_000010.10:g.112572544del , CM000672.1:g.112572544del	GRCh37
NC_000010.9:g.112562534del	NCBI36
NG_021177.1:g.173390del , LRG_382:g.173390del

Transcript Alleles

HGVS	Amino-acid change
ENST00000369519.4:c.2389del MANE Select	ENSP00000358532.3:p.His797IlefsTer?
ENST00000369519.3:c.2389del	ENSP00000358532.3:p.His797IlefsTer?
NM_001134363.2:c.2389del	NP_001127835.2:p.His797IlefsTer?
XM_011539697.1:c.2005del	XP_011537999.1:p.His669IlefsTer?
XM_017016103.2:c.2224del	XP_016871592.1:p.His742IlefsTer?
XM_017016104.2:c.2005del	XP_016871593.1:p.His669IlefsTer?
NM_001134363.3:c.2389del MANE Select	NP_001127835.2:p.His797IlefsTer?