Canonical Allele Identifier: CA399312540

Gene: ERBB2

Linked Data

• dbSNP Id: rs143958183
• MyVariant Identifiers: chr17:g.37883719C>G (hg19) ; chr17:g.39727466C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727466C>G , CM000679.2:g.39727466C>G	GRCh38
NC_000017.10:g.37883719C>G , CM000679.1:g.37883719C>G	GRCh37
NC_000017.9:g.35137245C>G	NCBI36
NG_007503.1:g.44327C>G , LRG_724:g.44327C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3331C>G MANE Select	ENSP00000269571.4:p.Arg1111Gly
ENST00000269571.9:c.3331C>G	ENSP00000269571.4:p.Arg1111Gly
ENST00000406381.6:c.3241C>G	ENSP00000385185.2:p.Arg1081Gly
ENST00000445658.6:c.2503C>G	ENSP00000404047.2:p.Arg835Gly
ENST00000541774.5:c.3286C>G	ENSP00000446466.1:p.Arg1096Gly
ENST00000578373.5:c.*3121C>G	ENSP00000463427.1:n.*3121C>G
ENST00000584450.5:c.3160-223C>G	ENSP00000463714.1:n.3160-223C>G
ENST00000584601.5:c.3241C>G	ENSP00000462438.1:p.Arg1081Gly
NM_001005862.2:c.3241C>G , LRG_724t1:c.3241C>G	NP_001005862.1:p.Arg1081Gly
NM_001289936.1:c.3286C>G , LRG_724t4:c.3286C>G	NP_001276865.1:p.Arg1096Gly
NM_001289937.1:c.3160-223C>G	NP_001276866.1:n.3160-223C>G
NM_004448.3:c.3331C>G , LRG_724t2:c.3331C>G	NP_004439.2:p.Arg1111Gly
NR_110535.1:n.3655C>G
XM_024450641.1:c.3469C>G	XP_024306409.1:p.Arg1157Gly
XM_024450642.1:c.3424C>G	XP_024306410.1:p.Arg1142Gly
XM_024450643.1:c.3379C>G	XP_024306411.1:p.Arg1127Gly
NM_001005862.3:c.3241C>G	NP_001005862.1:p.Arg1081Gly
NM_001289936.2:c.3286C>G	NP_001276865.1:p.Arg1096Gly
NM_001289937.2:c.3160-223C>G	NP_001276866.1:n.3160-223C>G
NM_001382782.1:c.3241C>G	NP_001369711.1:p.Arg1081Gly
NM_001382783.1:c.3241C>G	NP_001369712.1:p.Arg1081Gly
NM_001382784.1:c.3448C>G	NP_001369713.1:p.Arg1150Gly
NM_001382785.1:c.3433C>G	NP_001369714.1:p.Arg1145Gly
NM_001382786.1:c.3412C>G	NP_001369715.1:p.Arg1138Gly
NM_001382787.1:c.3406C>G	NP_001369716.1:p.Arg1136Gly
NM_001382788.1:c.3361C>G	NP_001369717.1:p.Arg1121Gly
NM_001382789.1:c.3352C>G	NP_001369718.1:p.Arg1118Gly
NM_001382790.1:c.3328C>G	NP_001369719.1:p.Arg1110Gly
NM_001382791.1:c.3322C>G	NP_001369720.1:p.Arg1108Gly
NM_001382792.1:c.3295C>G	NP_001369721.1:p.Arg1099Gly
NM_001382793.1:c.3289C>G	NP_001369722.1:p.Arg1097Gly
NM_001382794.1:c.3289C>G	NP_001369723.1:p.Arg1097Gly
NM_001382795.1:c.3283C>G	NP_001369724.1:p.Arg1095Gly
NM_001382796.1:c.3244C>G	NP_001369725.1:p.Arg1082Gly
NM_001382797.1:c.3232C>G	NP_001369726.1:p.Arg1078Gly
NM_001382798.1:c.3175C>G	NP_001369727.1:p.Arg1059Gly
NM_001382799.1:c.3151C>G	NP_001369728.1:p.Arg1051Gly
NM_001382800.1:c.3145C>G	NP_001369729.1:p.Arg1049Gly
NM_001382801.1:c.3127C>G	NP_001369730.1:p.Arg1043Gly
NM_001382802.1:c.3073C>G	NP_001369731.1:p.Arg1025Gly
NM_001382803.1:c.3118-223C>G	NP_001369732.1:n.3118-223C>G
NM_001382804.1:c.2503C>G	NP_001369733.1:p.Arg835Gly
NM_001382805.1:c.2380C>G	NP_001369734.1:p.Arg794Gly
NM_001382806.1:c.2293C>G	NP_001369735.1:p.Arg765Gly
NM_004448.4:c.3331C>G MANE Select	NP_004439.2:p.Arg1111Gly
NR_110535.2:n.3569C>G