Canonical Allele Identifier: CA1469632882

Gene: SHROOM3

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.76476985_76476986delinsTG , CM000666.2:g.76476985_76476986delinsTG	GRCh38
NC_000004.11:g.77398138_77398139delinsTG , CM000666.1:g.77398138_77398139delinsTG	GRCh37
NC_000004.10:g.77617162_77617163delinsTG	NCBI36
NG_028077.1:g.46886_46887delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296043.7:c.168+40765_168+40766delinsTG MANE Select	ENSP00000296043.6:n.168+40765_168+40766delinsTG
ENST00000296043.6:c.168+40765_168+40766delinsTG	ENSP00000296043.6:n.168+40765_168+40766delinsTG
ENST00000466541.1:n.75+40765_75+40766delinsTG
ENST00000497440.5:n.109+40765_109+40766delinsTG
NM_020859.3:c.168+40765_168+40766delinsTG	NP_065910.3:n.168+40765_168+40766delinsTG
XM_005263162.3:c.168+40765_168+40766delinsTG	XP_005263219.1:n.168+40765_168+40766delinsTG
XM_011532158.1:c.168+40765_168+40766delinsTG	XP_011530460.1:n.168+40765_168+40766delinsTG
XM_011532159.1:c.168+40765_168+40766delinsTG	XP_011530461.1:n.168+40765_168+40766delinsTG
XM_011532158.3:c.168+40765_168+40766delinsTG	XP_011530460.1:n.168+40765_168+40766delinsTG
NM_020859.4:c.168+40765_168+40766delinsTG MANE Select	NP_065910.3:n.168+40765_168+40766delinsTG