Canonical Allele Identifier: CA2695228821

Gene: RPS19

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41869109del , CM000681.2:g.41869109del	GRCh38
NC_000019.9:g.42373179del , CM000681.1:g.42373179del	GRCh37
NC_000019.8:g.47065019del	NCBI36
NG_007080.2:g.14192del
NG_007080.3:g.14192del

Transcript Alleles

HGVS	Amino-acid change
ENST00000598261.2:c.264del	ENSP00000469798.1:p.Lys89AsnfsTer?
ENST00000598742.6:c.251del MANE Select	ENSP00000470972.1:p.Arg84LysfsTer27
ENST00000600467.6:c.251del	ENSP00000469228.2:p.Arg84LysfsTer27
ENST00000221975.6:c.29del	ENSP00000221975.2:p.Arg10LysfsTer27
ENST00000593863.5:c.251del	ENSP00000470004.1:p.Arg84LysfsTer27
ENST00000598261.1:c.264del	ENSP00000469798.1:p.Lys89AsnfsTer?
ENST00000598399.1:c.1089del	ENSP00000472660.1:n.1089del
ENST00000598742.5:c.251del	ENSP00000470972.1:p.Arg84LysfsTer27
NM_001022.3:c.251del	NP_001013.1:p.Arg84LysfsTer27
NM_001321483.1:c.251del	NP_001308412.1:p.Arg84LysfsTer27
NM_001321484.1:c.251del	NP_001308413.1:p.Arg84LysfsTer27
NM_001321485.1:c.264del	NP_001308414.1:p.Lys89AsnfsTer?
XM_017027113.2:c.251del	XP_016882602.1:p.Arg84LysfsTer27
NM_001022.4:c.251del MANE Select	NP_001013.1:p.Arg84LysfsTer27
NM_001321483.2:c.251del	NP_001308412.1:p.Arg84LysfsTer27
NM_001321484.2:c.251del	NP_001308413.1:p.Arg84LysfsTer27
NM_001321485.2:c.264del	NP_001308414.1:p.Lys89AsnfsTer?