Canonical Allele Identifier: CA919838690

Gene: ERBB2

Linked Data

• dbSNP Id: rs1597886988

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39724952_39724953insGTTT , CM000679.2:g.39724952_39724953insGTTT	GRCh38
NC_000017.10:g.37881205_37881206insGTTT , CM000679.1:g.37881205_37881206insGTTT	GRCh37
NC_000017.9:g.35134731_35134732insGTTT	NCBI36
NG_007503.1:g.41813_41814insGTTT , LRG_724:g.41813_41814insGTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.2493+41_2493+42insGTTT MANE Select	ENSP00000269571.4:n.2493+41_2493+42insGTTT
ENST00000269571.9:c.2493+41_2493+42insGTTT	ENSP00000269571.4:n.2493+41_2493+42insGTTT
ENST00000406381.6:c.2403+41_2403+42insGTTT	ENSP00000385185.2:n.2403+41_2403+42insGTTT
ENST00000445658.6:c.1665+41_1665+42insGTTT	ENSP00000404047.2:n.1665+41_1665+42insGTTT
ENST00000541774.5:c.2448+41_2448+42insGTTT	ENSP00000446466.1:n.2448+41_2448+42insGTTT
ENST00000578373.5:c.*2283+41_*2283+42insGTTT	ENSP00000463427.1:n.*2283+41_*2283+42insGTTT
ENST00000580074.1:c.599+41_599+42insGTTT
ENST00000583038.5:n.3627+41_3627+42insGTTT
ENST00000584450.5:c.2493+41_2493+42insGTTT	ENSP00000463714.1:n.2493+41_2493+42insGTTT
ENST00000584601.5:c.2403+41_2403+42insGTTT	ENSP00000462438.1:n.2403+41_2403+42insGTTT
NM_001005862.2:c.2403+41_2403+42insGTTT , LRG_724t1:c.2403+41_2403+42insGTTT	NP_001005862.1:n.2403+41_2403+42insGTTT
NM_001289936.1:c.2448+41_2448+42insGTTT , LRG_724t4:c.2448+41_2448+42insGTTT	NP_001276865.1:n.2448+41_2448+42insGTTT
NM_001289937.1:c.2493+41_2493+42insGTTT	NP_001276866.1:n.2493+41_2493+42insGTTT
NM_004448.3:c.2493+41_2493+42insGTTT , LRG_724t2:c.2493+41_2493+42insGTTT	NP_004439.2:n.2493+41_2493+42insGTTT
NR_110535.1:n.2817+41_2817+42insGTTT
XM_024450641.1:c.2631+41_2631+42insGTTT	XP_024306409.1:n.2631+41_2631+42insGTTT
XM_024450642.1:c.2586+41_2586+42insGTTT	XP_024306410.1:n.2586+41_2586+42insGTTT
XM_024450643.1:c.2541+41_2541+42insGTTT	XP_024306411.1:n.2541+41_2541+42insGTTT
NM_001005862.3:c.2403+41_2403+42insGTTT	NP_001005862.1:n.2403+41_2403+42insGTTT
NM_001289936.2:c.2448+41_2448+42insGTTT	NP_001276865.1:n.2448+41_2448+42insGTTT
NM_001289937.2:c.2493+41_2493+42insGTTT	NP_001276866.1:n.2493+41_2493+42insGTTT
NM_001382782.1:c.2403+41_2403+42insGTTT	NP_001369711.1:n.2403+41_2403+42insGTTT
NM_001382783.1:c.2403+41_2403+42insGTTT	NP_001369712.1:n.2403+41_2403+42insGTTT
NM_001382784.1:c.2610+41_2610+42insGTTT	NP_001369713.1:n.2610+41_2610+42insGTTT
NM_001382785.1:c.2595+41_2595+42insGTTT	NP_001369714.1:n.2595+41_2595+42insGTTT
NM_001382786.1:c.2574+41_2574+42insGTTT	NP_001369715.1:n.2574+41_2574+42insGTTT
NM_001382787.1:c.2568+41_2568+42insGTTT	NP_001369716.1:n.2568+41_2568+42insGTTT
NM_001382788.1:c.2523+41_2523+42insGTTT	NP_001369717.1:n.2523+41_2523+42insGTTT
NM_001382789.1:c.2514+41_2514+42insGTTT	NP_001369718.1:n.2514+41_2514+42insGTTT
NM_001382790.1:c.2490+41_2490+42insGTTT	NP_001369719.1:n.2490+41_2490+42insGTTT
NM_001382791.1:c.2484+41_2484+42insGTTT	NP_001369720.1:n.2484+41_2484+42insGTTT
NM_001382792.1:c.2457+41_2457+42insGTTT	NP_001369721.1:n.2457+41_2457+42insGTTT
NM_001382793.1:c.2451+41_2451+42insGTTT	NP_001369722.1:n.2451+41_2451+42insGTTT
NM_001382794.1:c.2451+41_2451+42insGTTT	NP_001369723.1:n.2451+41_2451+42insGTTT
NM_001382795.1:c.2445+41_2445+42insGTTT	NP_001369724.1:n.2445+41_2445+42insGTTT
NM_001382796.1:c.2493+41_2493+42insGTTT	NP_001369725.1:n.2493+41_2493+42insGTTT
NM_001382797.1:c.2394+41_2394+42insGTTT	NP_001369726.1:n.2394+41_2394+42insGTTT
NM_001382798.1:c.2493+41_2493+42insGTTT	NP_001369727.1:n.2493+41_2493+42insGTTT
NM_001382799.1:c.2313+41_2313+42insGTTT	NP_001369728.1:n.2313+41_2313+42insGTTT
NM_001382800.1:c.2308-97_2308-96insGTTT	NP_001369729.1:n.2308-97_2308-96insGTTT
NM_001382801.1:c.2445+41_2445+42insGTTT	NP_001369730.1:n.2445+41_2445+42insGTTT
NM_001382802.1:c.2235+41_2235+42insGTTT	NP_001369731.1:n.2235+41_2235+42insGTTT
NM_001382803.1:c.2451+41_2451+42insGTTT	NP_001369732.1:n.2451+41_2451+42insGTTT
NM_001382804.1:c.1665+41_1665+42insGTTT	NP_001369733.1:n.1665+41_1665+42insGTTT
NM_001382805.1:c.2208+1292_2208+1293insGTTT	NP_001369734.1:n.2208+1292_2208+1293insGTTT
NM_001382806.1:c.1455+41_1455+42insGTTT	NP_001369735.1:n.1455+41_1455+42insGTTT
NM_004448.4:c.2493+41_2493+42insGTTT MANE Select	NP_004439.2:n.2493+41_2493+42insGTTT
NR_110535.2:n.2731+41_2731+42insGTTT