Canonical Allele Identifier: CA433169413

Linked Data

MyVariant Identifiers: chr3:g.39450023C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.39408532C>G , CM000665.2:g.39408532C>G GRCh38
NC_000003.11:g.39450023C>G , CM000665.1:g.39450023C>G GRCh37
NC_000003.10:g.39425027C>G NCBI36
NG_033234.1:g.6820C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000458478.6:c.134-74C>G (RPSA) ENSP00000410848.2:n.134-74C>G
ENST00000478027.3:n.610C>G (RPSA)
ENST00000697728.1:c.134-74C>G (RPSA) ENSP00000513422.1:n.134-74C>G
ENST00000697729.1:c.134-74C>G (RPSA) ENSP00000513423.1:n.134-74C>G
ENST00000697730.1:c.134-74C>G (RPSA) ENSP00000513424.1:n.134-74C>G
ENST00000697731.1:c.134-74C>G (RPSA) ENSP00000513425.1:n.134-74C>G
ENST00000697732.1:n.122-74C>G (RPSA)
ENST00000697753.1:c.134-74C>G (RPSA) ENSP00000513432.1:n.134-74C>G
ENST00000697816.1:c.*31-74C>G (RPSA) ENSP00000513451.1:n.*31-74C>G
ENST00000301821.11:c.134-74C>G (RPSA) MANE Select ENSP00000346067.4:n.134-74C>G
ENST00000301821.10:c.134-74C>G (RPSA) ENSP00000346067.4:n.134-74C>G
ENST00000443003.2:c.134-74C>G (RPSA) ENSP00000389351.1:n.134-74C>G
ENST00000444512.2:c.134-74C>G (RPSA) ENSP00000396716.2:n.134-74C>G
ENST00000458478.5:c.134-74C>G (RPSA) ENSP00000410848.1:n.134-74C>G
ENST00000477325.1:n.216-74C>G (RPSA)
ENST00000478027.2:n.329C>G (RPSA)
NM_001304288.1:c.134-74C>G (RPSA) NP_001291217.1:n.134-74C>G
NM_002295.5:c.134-74C>G (RPSA) NP_002286.2:n.134-74C>G
NR_002325.1:n.142C>G (SNORA6)
NM_002295.6:c.134-74C>G (RPSA) MANE Select NP_002286.2:n.134-74C>G
NM_001304288.2:c.134-74C>G (RPSA) NP_001291217.1:n.134-74C>G