Canonical Allele Identifier: CA1469632609
Gene: SHROOM3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.76476731G= , CM000666.2:g.76476731G= GRCh38
NC_000004.11:g.77397884G= , CM000666.1:g.77397884G= GRCh37
NC_000004.10:g.77616908G= NCBI36
NG_028077.1:g.46632G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000296043.7:c.168+40511G= MANE Select ENSP00000296043.6:n.168+40511G=
ENST00000296043.6:c.168+40511G= ENSP00000296043.6:n.168+40511G=
ENST00000466541.1:n.75+40511G=
ENST00000497440.5:n.109+40511G=
NM_020859.3:c.168+40511G= NP_065910.3:n.168+40511G=
XM_005263162.3:c.168+40511G= XP_005263219.1:n.168+40511G=
XM_011532158.1:c.168+40511G= XP_011530460.1:n.168+40511G=
XM_011532159.1:c.168+40511G= XP_011530461.1:n.168+40511G=
XM_011532158.3:c.168+40511G= XP_011530460.1:n.168+40511G=
NM_020859.4:c.168+40511G= MANE Select NP_065910.3:n.168+40511G=