Canonical Allele Identifier: CA1469632383

Gene: SHROOM3

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.76476525_76476526delinsAG , CM000666.2:g.76476525_76476526delinsAG	GRCh38
NC_000004.11:g.77397678_77397679delinsAG , CM000666.1:g.77397678_77397679delinsAG	GRCh37
NC_000004.10:g.77616702_77616703delinsAG	NCBI36
NG_028077.1:g.46426_46427delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296043.7:c.168+40305_168+40306delinsAG MANE Select	ENSP00000296043.6:n.168+40305_168+40306delinsAG
ENST00000296043.6:c.168+40305_168+40306delinsAG	ENSP00000296043.6:n.168+40305_168+40306delinsAG
ENST00000466541.1:n.75+40305_75+40306delinsAG
ENST00000497440.5:n.109+40305_109+40306delinsAG
NM_020859.3:c.168+40305_168+40306delinsAG	NP_065910.3:n.168+40305_168+40306delinsAG
XM_005263162.3:c.168+40305_168+40306delinsAG	XP_005263219.1:n.168+40305_168+40306delinsAG
XM_011532158.1:c.168+40305_168+40306delinsAG	XP_011530460.1:n.168+40305_168+40306delinsAG
XM_011532159.1:c.168+40305_168+40306delinsAG	XP_011530461.1:n.168+40305_168+40306delinsAG
XM_011532158.3:c.168+40305_168+40306delinsAG	XP_011530460.1:n.168+40305_168+40306delinsAG
NM_020859.4:c.168+40305_168+40306delinsAG MANE Select	NP_065910.3:n.168+40305_168+40306delinsAG