Canonical Allele Identifier: CA399310665

Gene: ERBB2

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3274A>G MANE Select	ENSP00000269571.4:p.Met1092Val
ENST00000269571.9:c.3274A>G	ENSP00000269571.4:p.Met1092Val
ENST00000406381.6:c.3184A>G	ENSP00000385185.2:p.Met1062Val
ENST00000445658.6:c.2446A>G	ENSP00000404047.2:p.Met816Val
ENST00000541774.5:c.3229A>G	ENSP00000446466.1:p.Met1077Val
ENST00000578373.5:c.*3064A>G	ENSP00000463427.1:n.*3064A>G
ENST00000584450.5:c.3160-280A>G	ENSP00000463714.1:n.3160-280A>G
ENST00000584601.5:c.3184A>G	ENSP00000462438.1:p.Met1062Val
NM_001005862.2:c.3184A>G , LRG_724t1:c.3184A>G	NP_001005862.1:p.Met1062Val
NM_001289936.1:c.3229A>G , LRG_724t4:c.3229A>G	NP_001276865.1:p.Met1077Val
NM_001289937.1:c.3160-280A>G	NP_001276866.1:n.3160-280A>G
NM_004448.3:c.3274A>G , LRG_724t2:c.3274A>G	NP_004439.2:p.Met1092Val
NR_110535.1:n.3598A>G
XM_024450641.1:c.3412A>G	XP_024306409.1:p.Met1138Val
XM_024450642.1:c.3367A>G	XP_024306410.1:p.Met1123Val
XM_024450643.1:c.3322A>G	XP_024306411.1:p.Met1108Val
NM_001005862.3:c.3184A>G	NP_001005862.1:p.Met1062Val
NM_001289936.2:c.3229A>G	NP_001276865.1:p.Met1077Val
NM_001289937.2:c.3160-280A>G	NP_001276866.1:n.3160-280A>G
NM_001382782.1:c.3184A>G	NP_001369711.1:p.Met1062Val
NM_001382783.1:c.3184A>G	NP_001369712.1:p.Met1062Val
NM_001382784.1:c.3391A>G	NP_001369713.1:p.Met1131Val
NM_001382785.1:c.3376A>G	NP_001369714.1:p.Met1126Val
NM_001382786.1:c.3355A>G	NP_001369715.1:p.Met1119Val
NM_001382787.1:c.3349A>G	NP_001369716.1:p.Met1117Val
NM_001382788.1:c.3304A>G	NP_001369717.1:p.Met1102Val
NM_001382789.1:c.3295A>G	NP_001369718.1:p.Met1099Val
NM_001382790.1:c.3271A>G	NP_001369719.1:p.Met1091Val
NM_001382791.1:c.3265A>G	NP_001369720.1:p.Met1089Val
NM_001382792.1:c.3238A>G	NP_001369721.1:p.Met1080Val
NM_001382793.1:c.3232A>G	NP_001369722.1:p.Met1078Val
NM_001382794.1:c.3232A>G	NP_001369723.1:p.Met1078Val
NM_001382795.1:c.3226A>G	NP_001369724.1:p.Met1076Val
NM_001382796.1:c.3187A>G	NP_001369725.1:p.Met1063Val
NM_001382797.1:c.3175A>G	NP_001369726.1:p.Met1059Val
NM_001382798.1:c.3118A>G	NP_001369727.1:p.Met1040Val
NM_001382799.1:c.3094A>G	NP_001369728.1:p.Met1032Val
NM_001382800.1:c.3088A>G	NP_001369729.1:p.Met1030Val
NM_001382801.1:c.3070A>G	NP_001369730.1:p.Met1024Val
NM_001382802.1:c.3016A>G	NP_001369731.1:p.Met1006Val
NM_001382803.1:c.3118-280A>G	NP_001369732.1:n.3118-280A>G
NM_001382804.1:c.2446A>G	NP_001369733.1:p.Met816Val
NM_001382805.1:c.2323A>G	NP_001369734.1:p.Met775Val
NM_001382806.1:c.2236A>G	NP_001369735.1:p.Met746Val
NM_004448.4:c.3274A>G MANE Select	NP_004439.2:p.Met1092Val
NR_110535.2:n.3512A>G