Canonical Allele Identifier: CA493801949
Community Standard Title: NM_001019.5(RPS15A):c.213G>A (p.Lys71=)
Gene: RPS15A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.18788063C>T , CM000678.2:g.18788063C>T GRCh38
NC_000016.9:g.18799385C>T , CM000678.1:g.18799385C>T GRCh37
NC_000016.8:g.18706886C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_001019.5:c.213G>A MANE Select NP_001010.2:p.Lys71=
ENST00000322989.8:c.213G>A MANE Select ENSP00000318646.4:p.Lys71=
NM_001019.4:c.213G>A NP_001010.2:p.Lys71=
NM_001030009.1:c.213G>A NP_001025180.1:p.Lys71=
NM_001030009.2:c.213G>A NP_001025180.1:p.Lys71=
ENST00000562935.5:c.*23G>A ENSP00000457001.1:n.*23G>A
ENST00000563390.5:c.213G>A ENSP00000457000.1:p.Lys71=
ENST00000565420.5:c.213G>A ENSP00000458115.1:p.Lys71=
ENST00000567078.2:c.711G>A ENSP00000454746.2:p.Lys237=
ENST00000569083.1:c.213G>A ENSP00000460618.1:p.Lys71=
ENST00000569365.6:c.*80G>A ENSP00000457924.2:n.*80G>A
ENST00000572008.5:c.213G>A ENSP00000458528.1:p.Lys71=
ENST00000574723.5:c.133+918G>A ENSP00000460069.1:n.133+918G>A
ENST00000576008.5:c.213G>A ENSP00000459373.1:p.Lys71=
ENST00000576436.5:c.213G>A ENSP00000459554.1:p.Lys71=