Canonical Allele Identifier: CA1469632617

Gene: SHROOM3

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.76476742_76476752delinsCTCTCCTTTCA , CM000666.2:g.76476742_76476752delinsCTCTCCTTTCA	GRCh38
NC_000004.11:g.77397895_77397905delinsCTCTCCTTTCA , CM000666.1:g.77397895_77397905delinsCTCTCCTTTCA	GRCh37
NC_000004.10:g.77616919_77616929delinsCTCTCCTTTCA	NCBI36
NG_028077.1:g.46643_46653delinsCTCTCCTTTCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296043.7:c.168+40522_168+40532delinsCTCTCCTTTCA MANE Select	ENSP00000296043.6:n.168+40522_168+40532delinsCTCTCCTTTCA
ENST00000296043.6:c.168+40522_168+40532delinsCTCTCCTTTCA	ENSP00000296043.6:n.168+40522_168+40532delinsCTCTCCTTTCA
ENST00000466541.1:n.75+40522_75+40532delinsCTCTCCTTTCA
ENST00000497440.5:n.109+40522_109+40532delinsCTCTCCTTTCA
NM_020859.3:c.168+40522_168+40532delinsCTCTCCTTTCA	NP_065910.3:n.168+40522_168+40532delinsCTCTCCTTTCA
XM_005263162.3:c.168+40522_168+40532delinsCTCTCCTTTCA	XP_005263219.1:n.168+40522_168+40532delinsCTCTCCTTTCA
XM_011532158.1:c.168+40522_168+40532delinsCTCTCCTTTCA	XP_011530460.1:n.168+40522_168+40532delinsCTCTCCTTTCA
XM_011532159.1:c.168+40522_168+40532delinsCTCTCCTTTCA	XP_011530461.1:n.168+40522_168+40532delinsCTCTCCTTTCA
XM_011532158.3:c.168+40522_168+40532delinsCTCTCCTTTCA	XP_011530460.1:n.168+40522_168+40532delinsCTCTCCTTTCA
NM_020859.4:c.168+40522_168+40532delinsCTCTCCTTTCA MANE Select	NP_065910.3:n.168+40522_168+40532delinsCTCTCCTTTCA