Canonical Allele Identifier: CA308568377

Gene: RPS19

Linked Data

• COSMIC: COSN18741589 ; COSN18741698
• MyVariant Identifiers: chr19:g.41869227del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41869227del , CM000681.2:g.41869227del	GRCh38
NC_000019.9:g.42373297del , CM000681.1:g.42373297del	GRCh37
NC_000019.8:g.47065137del	NCBI36
NG_007080.2:g.14310del
NG_007080.3:g.14310del

Transcript Alleles

HGVS	Amino-acid change
ENST00000598742.6:c.356+13del MANE Select	ENSP00000470972.1:n.356+13del
ENST00000600467.6:c.356+13del	ENSP00000469228.2:n.356+13del
ENST00000221975.6:c.134+13del	ENSP00000221975.2:n.134+13del
ENST00000593863.5:c.356+13del	ENSP00000470004.1:n.356+13del
ENST00000598742.5:c.356+13del	ENSP00000470972.1:n.356+13del
NM_001022.3:c.356+13del	NP_001013.1:n.356+13del
NM_001321483.1:c.356+13del	NP_001308412.1:n.356+13del
NM_001321484.1:c.356+13del	NP_001308413.1:n.356+13del
NM_001321485.1:c.369+13del	NP_001308414.1:n.369+13del
XM_017027113.2:c.356+13del	XP_016882602.1:n.356+13del
NM_001022.4:c.356+13del MANE Select	NP_001013.1:n.356+13del
NM_001321483.2:c.356+13del	NP_001308412.1:n.356+13del
NM_001321484.2:c.356+13del	NP_001308413.1:n.356+13del
NM_001321485.2:c.369+13del	NP_001308414.1:n.369+13del