Canonical Allele Identifier: CA2762255377
Gene: SHROOM3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.76476693dup , CM000666.2:g.76476693dup GRCh38
NC_000004.11:g.77397846dup , CM000666.1:g.77397846dup GRCh37
NC_000004.10:g.77616870dup NCBI36
NG_028077.1:g.46594dup

Transcript Alleles

HGVS Amino-acid change
ENST00000296043.7:c.168+40473dup MANE Select ENSP00000296043.6:n.168+40473dup
ENST00000296043.6:c.168+40473dup ENSP00000296043.6:n.168+40473dup
ENST00000466541.1:n.75+40473dup
ENST00000497440.5:n.109+40473dup
NM_020859.3:c.168+40473dup NP_065910.3:n.168+40473dup
XM_005263162.3:c.168+40473dup XP_005263219.1:n.168+40473dup
XM_011532158.1:c.168+40473dup XP_011530460.1:n.168+40473dup
XM_011532159.1:c.168+40473dup XP_011530461.1:n.168+40473dup
XM_011532158.3:c.168+40473dup XP_011530460.1:n.168+40473dup
NM_020859.4:c.168+40473dup MANE Select NP_065910.3:n.168+40473dup