Canonical Allele Identifier: CA2428933399
Gene: SHROOM4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.50635544T= , CM000685.2:g.50635544T= GRCh38
NC_000023.10:g.50378544T= , CM000685.1:g.50378544T= GRCh37
NC_000023.9:g.50395284T= NCBI36
NG_011882.1:g.183501A=

Transcript Alleles

HGVS Amino-acid change
ENST00000376020.9:c.529A= MANE Select ENSP00000365188.2:p.Ile177=
ENST00000376020.8:c.529A= ENSP00000365188.2:p.Ile177=
ENST00000289292.11:c.529A= ENSP00000289292.7:p.Ile177=
ENST00000376020.6:c.529A= ENSP00000365188.2:p.Ile177=
ENST00000460112.3:c.181A= ENSP00000421450.1:p.Ile61=
NM_020717.3:c.529A= NP_065768.2:p.Ile177=
NR_027121.1:n.555A=
XM_006724590.2:c.181A= XP_006724653.1:p.Ile61=
XM_006724591.2:c.55A= XP_006724654.1:p.Ile19=
XM_011530800.1:c.394A= XP_011529102.1:p.Ile132=
XM_011530801.1:c.529A= XP_011529103.1:p.Ile177=
XR_938367.1:n.647A=
XR_938368.1:n.647A=
XM_017029682.2:c.529A= XP_016885171.1:p.Ile177=
XM_017029683.1:c.394A= XP_016885172.1:p.Ile132=
XM_017029684.1:c.181A= XP_016885173.1:p.Ile61=
XM_017029685.2:c.529A= XP_016885174.1:p.Ile177=
XM_017029686.1:c.55A= XP_016885175.1:p.Ile19=
XM_017029687.2:c.529A= XP_016885176.1:p.Ile177=
XR_001755716.2:n.660A=
XR_001755717.2:n.660A=
XR_001755718.2:n.660A=
NM_020717.5:c.529A= MANE Select NP_065768.2:p.Ile177=
NR_027121.3:n.705A=
NR_172068.1:n.570A=
NR_172069.1:n.625A=
NR_172070.1:n.490A=