Canonical Allele Identifier: CA13164213

Gene: RPP30

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.90873142T>G , CM000672.2:g.90873142T>G	GRCh38
NC_000010.10:g.92632899T>G , CM000672.1:g.92632899T>G	GRCh37
NC_000010.9:g.92622879T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371703.8:c.82+1074T>G MANE Select	ENSP00000360768.3:n.82+1074T>G
ENST00000277882.7:c.148+1008T>G	ENSP00000277882.3:n.148+1008T>G
ENST00000371703.7:c.82+1074T>G	ENSP00000360768.3:n.82+1074T>G
ENST00000413330.5:c.82+1074T>G	ENSP00000389182.1:n.82+1074T>G
ENST00000487998.5:n.96+1074T>G
NM_001104546.1:c.82+1074T>G	NP_001098016.1:n.82+1074T>G
NM_006413.4:c.82+1074T>G	NP_006404.1:n.82+1074T>G
XM_011539120.1:c.82+1074T>G	XP_011537422.1:n.82+1074T>G
XM_011539121.1:c.82+1074T>G	XP_011537423.1:n.82+1074T>G
XM_011539122.1:c.82+1074T>G	XP_011537424.1:n.82+1074T>G
XM_011539123.1:c.82+1074T>G	XP_011537425.1:n.82+1074T>G
NM_001104546.2:c.82+1074T>G	NP_001098016.1:n.82+1074T>G
NM_006413.5:c.82+1074T>G MANE Select	NP_006404.1:n.82+1074T>G