Canonical Allele Identifier: CA2695228800

Gene: RPS19

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41869024_41869032del , CM000681.2:g.41869024_41869032del	GRCh38
NC_000019.9:g.42373094_42373102del , CM000681.1:g.42373094_42373102del	GRCh37
NC_000019.8:g.47064934_47064942del	NCBI36
NG_007080.2:g.14107_14115del
NG_007080.3:g.14107_14115del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000598261.2:c.186-7_187del
ENST00000598742.6:c.173-7_174del
ENST00000600467.6:c.173-7_174del
ENST00000221975.6:c.-50-7_-49del
ENST00000593863.5:c.173-7_174del
ENST00000598261.1:c.186-7_187del
ENST00000598399.1:c.1011-7_1012del
ENST00000598742.5:c.173-7_174del
ENST00000600467.5:c.173-7_174del
ENST00000601492.5:c.254-7_255del
NM_001022.3:c.173-7_174del
NM_001321483.1:c.173-7_174del
NM_001321484.1:c.173-7_174del
NM_001321485.1:c.186-7_187del
XM_017027113.2:c.173-7_174del
NM_001022.4:c.173-7_174del
NM_001321483.2:c.173-7_174del
NM_001321484.2:c.173-7_174del
NM_001321485.2:c.186-7_187del