Canonical Allele Identifier: CA406030348

Gene: RPS19

Linked Data

• MyVariant Identifiers: chr19:g.42373190A>C (hg19) ; chr19:g.41869120A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41869120A>C , CM000681.2:g.41869120A>C	GRCh38
NC_000019.9:g.42373190A>C , CM000681.1:g.42373190A>C	GRCh37
NC_000019.8:g.47065030A>C	NCBI36
NG_007080.2:g.14203A>C
NG_007080.3:g.14203A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000598261.2:c.275A>C	ENSP00000469798.1:p.His92Pro
ENST00000598742.6:c.262A>C MANE Select	ENSP00000470972.1:p.Met88Leu
ENST00000600467.6:c.262A>C	ENSP00000469228.2:p.Met88Leu
ENST00000221975.6:c.40A>C	ENSP00000221975.2:p.Met14Leu
ENST00000593863.5:c.262A>C	ENSP00000470004.1:p.Met88Leu
ENST00000598261.1:c.275A>C	ENSP00000469798.1:p.His92Pro
ENST00000598399.1:c.1100A>C	ENSP00000472660.1:n.1100A>C
ENST00000598742.5:c.262A>C	ENSP00000470972.1:p.Met88Leu
NM_001022.3:c.262A>C	NP_001013.1:p.Met88Leu
NM_001321483.1:c.262A>C	NP_001308412.1:p.Met88Leu
NM_001321484.1:c.262A>C	NP_001308413.1:p.Met88Leu
NM_001321485.1:c.275A>C	NP_001308414.1:p.His92Pro
XM_017027113.2:c.262A>C	XP_016882602.1:p.Met88Leu
NM_001022.4:c.262A>C MANE Select	NP_001013.1:p.Met88Leu
NM_001321483.2:c.262A>C	NP_001308412.1:p.Met88Leu
NM_001321484.2:c.262A>C	NP_001308413.1:p.Met88Leu
NM_001321485.2:c.275A>C	NP_001308414.1:p.His92Pro