Canonical Allele Identifier: CA399310666

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143244982
• MyVariant Identifiers: chr17:g.37883662A>T (hg19) ; chr17:g.39727409A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727409A>T , CM000679.2:g.39727409A>T	GRCh38
NC_000017.10:g.37883662A>T , CM000679.1:g.37883662A>T	GRCh37
NC_000017.9:g.35137188A>T	NCBI36
NG_007503.1:g.44270A>T , LRG_724:g.44270A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3274A>T MANE Select	ENSP00000269571.4:p.Met1092Leu
ENST00000269571.9:c.3274A>T	ENSP00000269571.4:p.Met1092Leu
ENST00000406381.6:c.3184A>T	ENSP00000385185.2:p.Met1062Leu
ENST00000445658.6:c.2446A>T	ENSP00000404047.2:p.Met816Leu
ENST00000541774.5:c.3229A>T	ENSP00000446466.1:p.Met1077Leu
ENST00000578373.5:c.*3064A>T	ENSP00000463427.1:n.*3064A>T
ENST00000584450.5:c.3160-280A>T	ENSP00000463714.1:n.3160-280A>T
ENST00000584601.5:c.3184A>T	ENSP00000462438.1:p.Met1062Leu
NM_001005862.2:c.3184A>T , LRG_724t1:c.3184A>T	NP_001005862.1:p.Met1062Leu
NM_001289936.1:c.3229A>T , LRG_724t4:c.3229A>T	NP_001276865.1:p.Met1077Leu
NM_001289937.1:c.3160-280A>T	NP_001276866.1:n.3160-280A>T
NM_004448.3:c.3274A>T , LRG_724t2:c.3274A>T	NP_004439.2:p.Met1092Leu
NR_110535.1:n.3598A>T
XM_024450641.1:c.3412A>T	XP_024306409.1:p.Met1138Leu
XM_024450642.1:c.3367A>T	XP_024306410.1:p.Met1123Leu
XM_024450643.1:c.3322A>T	XP_024306411.1:p.Met1108Leu
NM_001005862.3:c.3184A>T	NP_001005862.1:p.Met1062Leu
NM_001289936.2:c.3229A>T	NP_001276865.1:p.Met1077Leu
NM_001289937.2:c.3160-280A>T	NP_001276866.1:n.3160-280A>T
NM_001382782.1:c.3184A>T	NP_001369711.1:p.Met1062Leu
NM_001382783.1:c.3184A>T	NP_001369712.1:p.Met1062Leu
NM_001382784.1:c.3391A>T	NP_001369713.1:p.Met1131Leu
NM_001382785.1:c.3376A>T	NP_001369714.1:p.Met1126Leu
NM_001382786.1:c.3355A>T	NP_001369715.1:p.Met1119Leu
NM_001382787.1:c.3349A>T	NP_001369716.1:p.Met1117Leu
NM_001382788.1:c.3304A>T	NP_001369717.1:p.Met1102Leu
NM_001382789.1:c.3295A>T	NP_001369718.1:p.Met1099Leu
NM_001382790.1:c.3271A>T	NP_001369719.1:p.Met1091Leu
NM_001382791.1:c.3265A>T	NP_001369720.1:p.Met1089Leu
NM_001382792.1:c.3238A>T	NP_001369721.1:p.Met1080Leu
NM_001382793.1:c.3232A>T	NP_001369722.1:p.Met1078Leu
NM_001382794.1:c.3232A>T	NP_001369723.1:p.Met1078Leu
NM_001382795.1:c.3226A>T	NP_001369724.1:p.Met1076Leu
NM_001382796.1:c.3187A>T	NP_001369725.1:p.Met1063Leu
NM_001382797.1:c.3175A>T	NP_001369726.1:p.Met1059Leu
NM_001382798.1:c.3118A>T	NP_001369727.1:p.Met1040Leu
NM_001382799.1:c.3094A>T	NP_001369728.1:p.Met1032Leu
NM_001382800.1:c.3088A>T	NP_001369729.1:p.Met1030Leu
NM_001382801.1:c.3070A>T	NP_001369730.1:p.Met1024Leu
NM_001382802.1:c.3016A>T	NP_001369731.1:p.Met1006Leu
NM_001382803.1:c.3118-280A>T	NP_001369732.1:n.3118-280A>T
NM_001382804.1:c.2446A>T	NP_001369733.1:p.Met816Leu
NM_001382805.1:c.2323A>T	NP_001369734.1:p.Met775Leu
NM_001382806.1:c.2236A>T	NP_001369735.1:p.Met746Leu
NM_004448.4:c.3274A>T MANE Select	NP_004439.2:p.Met1092Leu
NR_110535.2:n.3512A>T