Canonical Allele Identifier: CA1469656175

Gene: SHROOM3

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.76499631C>A , CM000666.2:g.76499631C>A	GRCh38
NC_000004.11:g.77420784C>A , CM000666.1:g.77420784C>A	GRCh37
NC_000004.10:g.77639808C>A	NCBI36
NG_028077.1:g.69532C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296043.7:c.169-55978C>A MANE Select	ENSP00000296043.6:n.169-55978C>A
ENST00000296043.6:c.169-55978C>A	ENSP00000296043.6:n.169-55978C>A
ENST00000466541.1:n.76-55978C>A
ENST00000497440.5:n.110-55978C>A
NM_020859.3:c.169-55978C>A	NP_065910.3:n.169-55978C>A
XM_005263162.3:c.169-55978C>A	XP_005263219.1:n.169-55978C>A
XM_006714282.2:c.63+5109C>A	XP_006714345.1:n.63+5109C>A
XM_011532158.1:c.169-55975C>A	XP_011530460.1:n.169-55975C>A
XM_011532159.1:c.169-55975C>A	XP_011530461.1:n.169-55975C>A
XM_011532158.3:c.169-55975C>A	XP_011530460.1:n.169-55975C>A
XM_017008488.1:c.63+5109C>A	XP_016863977.1:n.63+5109C>A
XM_017008489.1:c.63+4999C>A	XP_016863978.1:n.63+4999C>A
NM_020859.4:c.169-55978C>A MANE Select	NP_065910.3:n.169-55978C>A