Canonical Allele Identifier: CA2610892489

Gene: RBM20

Linked Data

• gnomAD v4: 10-110810328-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.110810329del , CM000672.2:g.110810329del	GRCh38
NC_000010.10:g.112570087del , CM000672.1:g.112570087del	GRCh37
NC_000010.9:g.112560077del	NCBI36
NG_021177.1:g.170933del , LRG_382:g.170933del

Transcript Alleles

HGVS	Amino-acid change
ENST00000369519.4:c.1801-54del MANE Select	ENSP00000358532.3:n.1801-54del
ENST00000369519.3:c.1801-54del	ENSP00000358532.3:n.1801-54del
NM_001134363.2:c.1801-54del	NP_001127835.2:n.1801-54del
XM_011539697.1:c.1417-54del	XP_011537999.1:n.1417-54del
XM_017016103.2:c.1636-54del	XP_016871592.1:n.1636-54del
XM_017016104.2:c.1417-54del	XP_016871593.1:n.1417-54del
NM_001134363.3:c.1801-54del MANE Select	NP_001127835.2:n.1801-54del