Canonical Allele Identifier: CA1469632664
Gene: SHROOM3 HGNC NCBI

Linked Data

dbSNP Id: rs1731492945
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.76476762C>A , CM000666.2:g.76476762C>A GRCh38
NC_000004.11:g.77397915C>A , CM000666.1:g.77397915C>A GRCh37
NC_000004.10:g.77616939C>A NCBI36
NG_028077.1:g.46663C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000296043.7:c.168+40542C>A MANE Select ENSP00000296043.6:n.168+40542C>A
ENST00000296043.6:c.168+40542C>A ENSP00000296043.6:n.168+40542C>A
ENST00000466541.1:n.75+40542C>A
ENST00000497440.5:n.109+40542C>A
NM_020859.3:c.168+40542C>A NP_065910.3:n.168+40542C>A
XM_005263162.3:c.168+40542C>A XP_005263219.1:n.168+40542C>A
XM_011532158.1:c.168+40542C>A XP_011530460.1:n.168+40542C>A
XM_011532159.1:c.168+40542C>A XP_011530461.1:n.168+40542C>A
XM_011532158.3:c.168+40542C>A XP_011530460.1:n.168+40542C>A
NM_020859.4:c.168+40542C>A MANE Select NP_065910.3:n.168+40542C>A
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