Canonical Allele Identifier: CA10605779

Gene: SHROOM4

Linked Data

• ClinVar Variation Id: 287471
• ClinVar RCV Id: RCV000322654 ; RCV002494870
• dbSNP Id: rs886044870

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.50607728delinsCTCC , CM000685.2:g.50607728delinsCTCC	GRCh38
NC_000023.10:g.50350728delinsCTCC , CM000685.1:g.50350728delinsCTCC	GRCh37
NC_000023.9:g.50367468delinsCTCC	NCBI36
NG_011882.1:g.211317delinsGGAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376020.9:c.3414delinsGGAG MANE Select	ENSP00000365188.2:p.Glu1138_Glu1139insGlu
ENST00000376020.8:c.3414delinsGGAG	ENSP00000365188.2:p.Glu1138_Glu1139insGlu
ENST00000289292.11:c.3414delinsGGAG	ENSP00000289292.7:p.Glu1138_Glu1139insGlu
ENST00000376020.6:c.3414delinsGGAG	ENSP00000365188.2:p.Glu1138_Glu1139insGlu
ENST00000460112.3:c.3066delinsGGAG	ENSP00000421450.1:p.Glu1022_Glu1023insGlu
NM_020717.3:c.3414delinsGGAG	NP_065768.2:p.Glu1138_Glu1139insGlu
NR_027121.1:n.3440delinsGGAG
XM_006724590.2:c.3066delinsGGAG	XP_006724653.1:p.Glu1022_Glu1023insGlu
XM_006724591.2:c.2940delinsGGAG	XP_006724654.1:p.Glu980_Glu981insGlu
XM_011530800.1:c.3279delinsGGAG	XP_011529102.1:p.Glu1093_Glu1094insGlu
XM_011530801.1:c.3414delinsGGAG	XP_011529103.1:p.Glu1138_Glu1139insGlu
XR_938367.1:n.3532delinsGGAG
XR_938368.1:n.3532delinsGGAG
XM_017029682.2:c.3528delinsGGAG	XP_016885171.1:p.Glu1176_Glu1177insGlu
XM_017029683.1:c.3393delinsGGAG	XP_016885172.1:p.Glu1131_Glu1132insGlu
XM_017029684.1:c.3180delinsGGAG	XP_016885173.1:p.Glu1060_Glu1061insGlu
XM_017029685.2:c.3528delinsGGAG	XP_016885174.1:p.Glu1176_Glu1177insGlu
XM_017029686.1:c.3054delinsGGAG	XP_016885175.1:p.Glu1018_Glu1019insGlu
XR_001755716.2:n.3659delinsGGAG
XR_001755717.2:n.3659delinsGGAG
XR_001755718.2:n.3659delinsGGAG
NM_020717.5:c.3414delinsGGAG MANE Select	NP_065768.2:p.Glu1138_Glu1139insGlu
NR_027121.3:n.3590delinsGGAG
NR_172068.1:n.3455delinsGGAG
NR_172069.1:n.3510delinsGGAG
NR_172070.1:n.3375delinsGGAG