Canonical Allele Identifier: CA1469632707
Gene: SHROOM3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.76476811A= , CM000666.2:g.76476811A= GRCh38
NC_000004.11:g.77397964A= , CM000666.1:g.77397964A= GRCh37
NC_000004.10:g.77616988A= NCBI36
NG_028077.1:g.46712A=

Transcript Alleles

HGVS Amino-acid change
ENST00000296043.7:c.168+40591A= MANE Select ENSP00000296043.6:n.168+40591A=
ENST00000296043.6:c.168+40591A= ENSP00000296043.6:n.168+40591A=
ENST00000466541.1:n.75+40591A=
ENST00000497440.5:n.109+40591A=
NM_020859.3:c.168+40591A= NP_065910.3:n.168+40591A=
XM_005263162.3:c.168+40591A= XP_005263219.1:n.168+40591A=
XM_011532158.1:c.168+40591A= XP_011530460.1:n.168+40591A=
XM_011532159.1:c.168+40591A= XP_011530461.1:n.168+40591A=
XM_011532158.3:c.168+40591A= XP_011530460.1:n.168+40591A=
NM_020859.4:c.168+40591A= MANE Select NP_065910.3:n.168+40591A=