Canonical Allele Identifier: CA1469632720
Gene: SHROOM3 HGNC NCBI

Linked Data

dbSNP Id: rs1731493825
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.76476824_76476826del , CM000666.2:g.76476824_76476826del GRCh38
NC_000004.11:g.77397977_77397979del , CM000666.1:g.77397977_77397979del GRCh37
NC_000004.10:g.77617001_77617003del NCBI36
NG_028077.1:g.46725_46727del

Transcript Alleles

HGVS Amino-acid change
ENST00000296043.7:c.168+40604_168+40606del MANE Select ENSP00000296043.6:n.168+40604_168+40606de...
ENST00000296043.6:c.168+40604_168+40606del ENSP00000296043.6:n.168+40604_168+40606de...
ENST00000466541.1:n.75+40604_75+40606del
ENST00000497440.5:n.109+40604_109+40606del
NM_020859.3:c.168+40604_168+40606del NP_065910.3:n.168+40604_168+40606del
XM_005263162.3:c.168+40604_168+40606del XP_005263219.1:n.168+40604_168+40606del
XM_011532158.1:c.168+40604_168+40606del XP_011530460.1:n.168+40604_168+40606del
XM_011532159.1:c.168+40604_168+40606del XP_011530461.1:n.168+40604_168+40606del
XM_011532158.3:c.168+40604_168+40606del XP_011530460.1:n.168+40604_168+40606del
NM_020859.4:c.168+40604_168+40606del MANE Select NP_065910.3:n.168+40604_168+40606del
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