Canonical Allele Identifier: CA2972667

Gene: SHROOM3

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.76741095G>A , CM000666.2:g.76741095G>A	GRCh38
NC_000004.11:g.77662248G>A , CM000666.1:g.77662248G>A	GRCh37
NC_000004.10:g.77881272G>A	NCBI36
NG_028077.1:g.310996G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296043.7:c.2922G>A MANE Select	ENSP00000296043.6:p.Ser974=
ENST00000646790.1:c.2679G>A	ENSP00000494970.1:p.Ser893=
ENST00000296043.6:c.2922G>A	ENSP00000296043.6:p.Ser974=
ENST00000469923.5:n.415-7922G>A
ENST00000486758.5:n.2731G>A
NM_020859.3:c.2922G>A	NP_065910.3:p.Ser974=
XM_005263162.3:c.2922G>A	XP_005263219.1:p.Ser974=
XM_005263163.3:c.2394G>A	XP_005263220.1:p.Ser798=
XM_005263164.3:c.2394G>A	XP_005263221.1:p.Ser798=
XM_005263165.3:c.2394G>A	XP_005263222.1:p.Ser798=
XM_006714282.2:c.2817G>A	XP_006714345.1:p.Ser939=
XM_011532157.1:c.2679G>A	XP_011530459.1:p.Ser893=
XM_011532158.1:c.2925G>A	XP_011530460.1:p.Ser975=
XM_011532159.1:c.2925G>A	XP_011530461.1:p.Ser975=
XM_011532160.1:c.2547G>A	XP_011530462.1:p.Ser849=
XM_011532161.1:c.2394G>A	XP_011530463.1:p.Ser798=
XM_005263163.4:c.2394G>A	XP_005263220.1:p.Ser798=
XM_005263164.4:c.2394G>A	XP_005263221.1:p.Ser798=
XM_005263165.5:c.2394G>A	XP_005263222.1:p.Ser798=
XM_011532157.2:c.2940G>A	XP_011530459.2:p.Ser980=
XM_011532158.3:c.2925G>A	XP_011530460.1:p.Ser975=
XM_011532161.2:c.2394G>A	XP_011530463.1:p.Ser798=
XM_017008488.1:c.2820G>A	XP_016863977.1:p.Ser940=
XM_017008489.1:c.2817G>A	XP_016863978.1:p.Ser939=
NM_020859.4:c.2922G>A MANE Select	NP_065910.3:p.Ser974=