Canonical Allele Identifier: CA2610892666

Gene: RBM20

Linked Data

• gnomAD v4: 10-110812138-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.110812140del , CM000672.2:g.110812140del	GRCh38
NC_000010.10:g.112571898del , CM000672.1:g.112571898del	GRCh37
NC_000010.9:g.112561888del	NCBI36
NG_021177.1:g.172744del , LRG_382:g.172744del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369519.4:c.1881-138del MANE Select	ENSP00000358532.3:n.1881-138del
ENST00000369519.3:c.1881-138del	ENSP00000358532.3:n.1881-138del
NM_001134363.2:c.1881-138del	NP_001127835.2:n.1881-138del
XM_011539697.1:c.1497-138del	XP_011537999.1:n.1497-138del
XM_017016103.2:c.1716-138del	XP_016871592.1:n.1716-138del
XM_017016104.2:c.1497-138del	XP_016871593.1:n.1497-138del
NM_001134363.3:c.1881-138del MANE Select	NP_001127835.2:n.1881-138del