Canonical Allele Identifier: CA16620855
Gene: RPS19 HGNC NCBI

Linked Data

dbSNP Id: rs1064794604

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41869196_41869198del , CM000681.2:g.41869196_41869198del GRCh38
NC_000019.9:g.42373266_42373268del , CM000681.1:g.42373266_42373268del GRCh37
NC_000019.8:g.47065106_47065108del NCBI36
NG_007080.2:g.14279_14281del
NG_007080.3:g.14279_14281del

Transcript Alleles

HGVS Amino-acid change
ENST00000598742.6:c.338_340del MANE Select ENSP00000470972.1:p.Val113del
ENST00000600467.6:c.338_340del ENSP00000469228.2:p.Val113del
ENST00000221975.6:c.116_118del ENSP00000221975.2:p.Val39del
ENST00000593863.5:c.338_340del ENSP00000470004.1:p.Val113del
ENST00000598742.5:c.338_340del ENSP00000470972.1:p.Val113del
NM_001022.3:c.338_340del NP_001013.1:p.Val113del
NM_001321483.1:c.338_340del NP_001308412.1:p.Val113del
NM_001321484.1:c.338_340del NP_001308413.1:p.Val113del
NM_001321485.1:c.351_353del NP_001308414.1:p.Gly118del
XM_017027113.2:c.338_340del XP_016882602.1:p.Val113del
NM_001022.4:c.338_340del MANE Select NP_001013.1:p.Val113del
NM_001321483.2:c.338_340del NP_001308412.1:p.Val113del
NM_001321484.2:c.338_340del NP_001308413.1:p.Val113del
NM_001321485.2:c.351_353del NP_001308414.1:p.Gly118del