Canonical Allele Identifier: CA2576254902

Gene: ERBB2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727347_39727349del , CM000679.2:g.39727347_39727349del	GRCh38
NC_000017.10:g.37883600_37883602del , CM000679.1:g.37883600_37883602del	GRCh37
NC_000017.9:g.35137126_35137128del	NCBI36
NG_007503.1:g.44208_44210del , LRG_724:g.44208_44210del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3212_3214del MANE Select	ENSP00000269571.4:p.Pro1071del
ENST00000269571.9:c.3212_3214del	ENSP00000269571.4:p.Pro1071del
ENST00000406381.6:c.3122_3124del	ENSP00000385185.2:p.Pro1041del
ENST00000445658.6:c.2384_2386del	ENSP00000404047.2:p.Pro795del
ENST00000541774.5:c.3167_3169del	ENSP00000446466.1:p.Pro1056del
ENST00000578373.5:c.*3002_*3004del	ENSP00000463427.1:n.*3002_*3004del
ENST00000584450.5:c.3160-342_3160-340del	ENSP00000463714.1:n.3160-342_3160-340del
ENST00000584601.5:c.3122_3124del	ENSP00000462438.1:p.Pro1041del
NM_001005862.2:c.3122_3124del , LRG_724t1:c.3122_3124del	NP_001005862.1:p.Pro1041del
NM_001289936.1:c.3167_3169del , LRG_724t4:c.3167_3169del	NP_001276865.1:p.Pro1056del
NM_001289937.1:c.3160-342_3160-340del	NP_001276866.1:n.3160-342_3160-340del
NM_004448.3:c.3212_3214del , LRG_724t2:c.3212_3214del	NP_004439.2:p.Pro1071del
NR_110535.1:n.3536_3538del
XM_024450641.1:c.3350_3352del	XP_024306409.1:p.Pro1117del
XM_024450642.1:c.3305_3307del	XP_024306410.1:p.Pro1102del
XM_024450643.1:c.3260_3262del	XP_024306411.1:p.Pro1087del
NM_001005862.3:c.3122_3124del	NP_001005862.1:p.Pro1041del
NM_001289936.2:c.3167_3169del	NP_001276865.1:p.Pro1056del
NM_001289937.2:c.3160-342_3160-340del	NP_001276866.1:n.3160-342_3160-340del
NM_001382782.1:c.3122_3124del	NP_001369711.1:p.Pro1041del
NM_001382783.1:c.3122_3124del	NP_001369712.1:p.Pro1041del
NM_001382784.1:c.3329_3331del	NP_001369713.1:p.Pro1110del
NM_001382785.1:c.3314_3316del	NP_001369714.1:p.Pro1105del
NM_001382786.1:c.3293_3295del	NP_001369715.1:p.Pro1098del
NM_001382787.1:c.3287_3289del	NP_001369716.1:p.Pro1096del
NM_001382788.1:c.3242_3244del	NP_001369717.1:p.Pro1081del
NM_001382789.1:c.3233_3235del	NP_001369718.1:p.Pro1078del
NM_001382790.1:c.3209_3211del	NP_001369719.1:p.Pro1070del
NM_001382791.1:c.3203_3205del	NP_001369720.1:p.Pro1068del
NM_001382792.1:c.3176_3178del	NP_001369721.1:p.Pro1059del
NM_001382793.1:c.3170_3172del	NP_001369722.1:p.Pro1057del
NM_001382794.1:c.3170_3172del	NP_001369723.1:p.Pro1057del
NM_001382795.1:c.3164_3166del	NP_001369724.1:p.Pro1055del
NM_001382796.1:c.3125_3127del	NP_001369725.1:p.Pro1042del
NM_001382797.1:c.3113_3115del	NP_001369726.1:p.Pro1038del
NM_001382798.1:c.3056_3058del	NP_001369727.1:p.Pro1019del
NM_001382799.1:c.3032_3034del	NP_001369728.1:p.Pro1011del
NM_001382800.1:c.3026_3028del	NP_001369729.1:p.Pro1009del
NM_001382801.1:c.3008_3010del	NP_001369730.1:p.Pro1003del
NM_001382802.1:c.2954_2956del	NP_001369731.1:p.Pro985del
NM_001382803.1:c.3118-342_3118-340del	NP_001369732.1:n.3118-342_3118-340del
NM_001382804.1:c.2384_2386del	NP_001369733.1:p.Pro795del
NM_001382805.1:c.2261_2263del	NP_001369734.1:p.Pro754del
NM_001382806.1:c.2174_2176del	NP_001369735.1:p.Pro725del
NM_004448.4:c.3212_3214del MANE Select	NP_004439.2:p.Pro1071del
NR_110535.2:n.3450_3452del