Canonical Allele Identifier: CA206011

Gene: LARP7 MIR302CHG

Linked Data

• ClinVar Variation Id: 211371
• ClinVar RCV Id: RCV000192883
• dbSNP Id: rs1554011754
• MyVariant Identifiers: chr4:g.113568510_113569257del (hg19) ; chr4:g.112647354_112648101del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.112647354_112648101del , CM000666.2:g.112647354_112648101del	GRCh38
NC_000004.11:g.113568510_113569257del , CM000666.1:g.113568510_113569257del	GRCh37
NC_000004.10:g.113787959_113788706del	NCBI36
NG_032779.1:g.15391_16138del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000505034.6:c.802_1142+267del (LARP7)
ENST00000505216.2:c.*561_*901+267del (LARP7)
ENST00000694891.1:c.799_1139+267del (LARP7)
ENST00000694894.1:c.802_1142+267del (LARP7)
ENST00000694895.1:c.802_1142+267del (LARP7)
ENST00000694896.1:c.802_1181+267del (LARP7)
ENST00000694897.1:c.*201_*541+267del (LARP7)
ENST00000694898.1:c.802_1181+267del (LARP7)
ENST00000694899.1:c.799_1139+267del (LARP7)
ENST00000694900.1:c.802_1136+267del (LARP7)
ENST00000694901.1:c.*561_*901+267del (LARP7)
ENST00000511529.2:c.799_1178+267del (LARP7)
ENST00000512361.2:n.982_1322+267del (LARP7)
ENST00000512589.6:c.*608_*948+267del (LARP7)
ENST00000684864.1:c.802_1142+267del (LARP7)
ENST00000688617.1:n.1076_1416+267del (LARP7)
ENST00000689262.1:n.1953_2293+267del (LARP7)
ENST00000689844.1:c.802_1181+267del (LARP7)
ENST00000690008.1:c.*561_*901+267del (LARP7)
ENST00000692075.1:n.1038_1378+267del (LARP7)
ENST00000692168.1:n.968_1308+267del (LARP7)
ENST00000692416.1:c.565_905+267del (LARP7)
ENST00000693375.1:c.565_905+267del (LARP7)
ENST00000693442.1:c.802_1142+267del (LARP7)
ENST00000344442.10:c.802_1142+267del (LARP7)
ENST00000651579.1:c.802_1142+267del (LARP7)
ENST00000324052.10:c.802_1142+267del (LARP7)
ENST00000344442.9:c.802_1142+267del (LARP7)
ENST00000509061.5:c.823_1163+267del (LARP7)
ENST00000509622.5:c.*561_*901+267del (LARP7)
ENST00000511529.1:c.144_523+267del (LARP7)
ENST00000513553.5:c.31-365_146+267del (LARP7)
NM_001267039.1:c.823_1163+267del (LARP7)
NM_015454.2:c.802_1142+267del (LARP7)
NM_016648.3:c.802_1142+267del (LARP7)
NR_049768.1:n.977_1317+267del (LARP7)
NR_146092.1:n.147+414_148-384del (MIR302CHG)
NR_146093.1:n.50+555_103+63del (MIR302CHG)
NR_146094.1:n.50+555_51-384del (MIR302CHG)
XM_024454080.1:c.802_1181+267del (LARP7)
XM_024454081.1:c.802_1181+267del (LARP7)
XM_024454082.1:c.802_1181+267del (LARP7)
XM_024454083.1:c.802_1181+267del (LARP7)
XM_024454084.1:c.802_1142+267del (LARP7)
XM_024454085.1:c.802_1142+267del (LARP7)
XM_024454086.1:c.565_944+267del (LARP7)
XM_024454087.1:c.565_944+267del (LARP7)
XM_024454088.1:c.565_905+267del (LARP7)
XM_024454089.1:c.121_500+267del (LARP7)
NM_016648.4:c.802_1142+267del (LARP7)
NM_001370974.1:c.802_1181+267del (LARP7)
NM_001370975.1:c.802_1181+267del (LARP7)
NM_001370976.1:c.799_1178+267del (LARP7)
NM_001370977.1:c.799_1178+267del (LARP7)
NM_001370978.1:c.802_1142+267del (LARP7)
NM_001370979.1:c.799_1139+267del (LARP7)
NM_001370980.1:c.799_1139+267del (LARP7)
NM_001370981.1:c.565_905+267del (LARP7)
NM_001370982.1:c.565_905+267del (LARP7)
NM_001267039.2:c.823_1163+267del (LARP7)
NM_015454.3:c.802_1142+267del (LARP7)
NM_001267039.4:c.802_1142+267del (LARP7)