Canonical Allele Identifier: CA1469754248

Gene: SHROOM3 SHROOM3-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.76754352C= , CM000666.2:g.76754352C=	GRCh38
NC_000004.11:g.77675505C= , CM000666.1:g.77675505C=	GRCh37
NC_000004.10:g.77894529C=	NCBI36
NG_028077.1:g.324253C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296043.7:c.3869C= (SHROOM3) MANE Select	ENSP00000296043.6:p.Pro1290=
ENST00000646790.1:c.3626C= (SHROOM3)	ENSP00000494970.1:p.Pro1209=
ENST00000296043.6:c.3869C= (SHROOM3)	ENSP00000296043.6:p.Pro1290=
ENST00000469923.5:n.530C= (SHROOM3)
NM_020859.3:c.3869C= (SHROOM3)	NP_065910.3:p.Pro1290=
XM_005263162.3:c.3869C= (SHROOM3)	XP_005263219.1:p.Pro1290=
XM_005263163.3:c.3341C= (SHROOM3)	XP_005263220.1:p.Pro1114=
XM_005263164.3:c.3341C= (SHROOM3)	XP_005263221.1:p.Pro1114=
XM_005263165.3:c.3341C= (SHROOM3)	XP_005263222.1:p.Pro1114=
XM_006714282.2:c.3764C= (SHROOM3)	XP_006714345.1:p.Pro1255=
XM_011532157.1:c.3626C= (SHROOM3)	XP_011530459.1:p.Pro1209=
XM_011532158.1:c.3872C= (SHROOM3)	XP_011530460.1:p.Pro1291=
XM_011532159.1:c.3872C= (SHROOM3)	XP_011530461.1:p.Pro1291=
XM_011532160.1:c.3494C= (SHROOM3)	XP_011530462.1:p.Pro1165=
XM_011532161.1:c.3341C= (SHROOM3)	XP_011530463.1:p.Pro1114=
XR_938901.1:n.1465+3244G= (SHROOM3-AS1)
XR_938903.1:n.1012+3697G= (SHROOM3-AS1)
XM_005263163.4:c.3341C= (SHROOM3)	XP_005263220.1:p.Pro1114=
XM_005263164.4:c.3341C= (SHROOM3)	XP_005263221.1:p.Pro1114=
XM_005263165.5:c.3341C= (SHROOM3)	XP_005263222.1:p.Pro1114=
XM_011532157.2:c.3887C= (SHROOM3)	XP_011530459.2:p.Pro1296=
XM_011532158.3:c.3872C= (SHROOM3)	XP_011530460.1:p.Pro1291=
XM_011532161.2:c.3341C= (SHROOM3)	XP_011530463.1:p.Pro1114=
XM_017008488.1:c.3767C= (SHROOM3)	XP_016863977.1:p.Pro1256=
XM_017008489.1:c.3764C= (SHROOM3)	XP_016863978.1:p.Pro1255=
XR_001741405.1:n.393+3244G= (SHROOM3-AS1)
XR_002959829.1:n.1514+3244G= (SHROOM3-AS1)
XR_938903.2:n.1061+3697G= (SHROOM3-AS1)
NM_020859.4:c.3869C= (SHROOM3) MANE Select	NP_065910.3:p.Pro1290=