Canonical Allele Identifier: CA507576387

Gene: RPS19

Linked Data

• gnomAD v4: 19-41869176-C-T
• MyVariant Identifiers: chr19:g.42373246C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41869176C>T , CM000681.2:g.41869176C>T	GRCh38
NC_000019.9:g.42373246C>T , CM000681.1:g.42373246C>T	GRCh37
NC_000019.8:g.47065086C>T	NCBI36
NG_007080.2:g.14259C>T
NG_007080.3:g.14259C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000598742.6:c.318C>T MANE Select	ENSP00000470972.1:p.Ala106=
ENST00000600467.6:c.318C>T	ENSP00000469228.2:p.Ala106=
ENST00000221975.6:c.96C>T	ENSP00000221975.2:p.Ala32=
ENST00000593863.5:c.318C>T	ENSP00000470004.1:p.Ala106=
ENST00000598399.1:c.1156C>T	ENSP00000472660.1:n.1156C>T
ENST00000598742.5:c.318C>T	ENSP00000470972.1:p.Ala106=
NM_001022.3:c.318C>T	NP_001013.1:p.Ala106=
NM_001321483.1:c.318C>T	NP_001308412.1:p.Ala106=
NM_001321484.1:c.318C>T	NP_001308413.1:p.Ala106=
NM_001321485.1:c.331C>T	NP_001308414.1:p.Pro111Ser
XM_017027113.2:c.318C>T	XP_016882602.1:p.Ala106=
NM_001022.4:c.318C>T MANE Select	NP_001013.1:p.Ala106=
NM_001321483.2:c.318C>T	NP_001308412.1:p.Ala106=
NM_001321484.2:c.318C>T	NP_001308413.1:p.Ala106=
NM_001321485.2:c.331C>T	NP_001308414.1:p.Pro111Ser