Canonical Allele Identifier: CA399312676

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37883752T>G (hg19) ; chr17:g.39727499T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727499T>G , CM000679.2:g.39727499T>G	GRCh38
NC_000017.10:g.37883752T>G , CM000679.1:g.37883752T>G	GRCh37
NC_000017.9:g.35137278T>G	NCBI36
NG_007503.1:g.44360T>G , LRG_724:g.44360T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3364T>G MANE Select	ENSP00000269571.4:p.Ser1122Ala
ENST00000269571.9:c.3364T>G	ENSP00000269571.4:p.Ser1122Ala
ENST00000406381.6:c.3274T>G	ENSP00000385185.2:p.Ser1092Ala
ENST00000445658.6:c.2536T>G	ENSP00000404047.2:p.Ser846Ala
ENST00000541774.5:c.3319T>G	ENSP00000446466.1:p.Ser1107Ala
ENST00000578373.5:c.*3154T>G	ENSP00000463427.1:n.*3154T>G
ENST00000584450.5:c.3160-190T>G	ENSP00000463714.1:n.3160-190T>G
ENST00000584601.5:c.3274T>G	ENSP00000462438.1:p.Ser1092Ala
NM_001005862.2:c.3274T>G , LRG_724t1:c.3274T>G	NP_001005862.1:p.Ser1092Ala
NM_001289936.1:c.3319T>G , LRG_724t4:c.3319T>G	NP_001276865.1:p.Ser1107Ala
NM_001289937.1:c.3160-190T>G	NP_001276866.1:n.3160-190T>G
NM_004448.3:c.3364T>G , LRG_724t2:c.3364T>G	NP_004439.2:p.Ser1122Ala
NR_110535.1:n.3688T>G
XM_024450641.1:c.3502T>G	XP_024306409.1:p.Ser1168Ala
XM_024450642.1:c.3457T>G	XP_024306410.1:p.Ser1153Ala
XM_024450643.1:c.3412T>G	XP_024306411.1:p.Ser1138Ala
NM_001005862.3:c.3274T>G	NP_001005862.1:p.Ser1092Ala
NM_001289936.2:c.3319T>G	NP_001276865.1:p.Ser1107Ala
NM_001289937.2:c.3160-190T>G	NP_001276866.1:n.3160-190T>G
NM_001382782.1:c.3274T>G	NP_001369711.1:p.Ser1092Ala
NM_001382783.1:c.3274T>G	NP_001369712.1:p.Ser1092Ala
NM_001382784.1:c.3481T>G	NP_001369713.1:p.Ser1161Ala
NM_001382785.1:c.3466T>G	NP_001369714.1:p.Ser1156Ala
NM_001382786.1:c.3445T>G	NP_001369715.1:p.Ser1149Ala
NM_001382787.1:c.3439T>G	NP_001369716.1:p.Ser1147Ala
NM_001382788.1:c.3394T>G	NP_001369717.1:p.Ser1132Ala
NM_001382789.1:c.3385T>G	NP_001369718.1:p.Ser1129Ala
NM_001382790.1:c.3361T>G	NP_001369719.1:p.Ser1121Ala
NM_001382791.1:c.3355T>G	NP_001369720.1:p.Ser1119Ala
NM_001382792.1:c.3328T>G	NP_001369721.1:p.Ser1110Ala
NM_001382793.1:c.3322T>G	NP_001369722.1:p.Ser1108Ala
NM_001382794.1:c.3322T>G	NP_001369723.1:p.Ser1108Ala
NM_001382795.1:c.3316T>G	NP_001369724.1:p.Ser1106Ala
NM_001382796.1:c.3277T>G	NP_001369725.1:p.Ser1093Ala
NM_001382797.1:c.3265T>G	NP_001369726.1:p.Ser1089Ala
NM_001382798.1:c.3208T>G	NP_001369727.1:p.Ser1070Ala
NM_001382799.1:c.3184T>G	NP_001369728.1:p.Ser1062Ala
NM_001382800.1:c.3178T>G	NP_001369729.1:p.Ser1060Ala
NM_001382801.1:c.3160T>G	NP_001369730.1:p.Ser1054Ala
NM_001382802.1:c.3106T>G	NP_001369731.1:p.Ser1036Ala
NM_001382803.1:c.3118-190T>G	NP_001369732.1:n.3118-190T>G
NM_001382804.1:c.2536T>G	NP_001369733.1:p.Ser846Ala
NM_001382805.1:c.2413T>G	NP_001369734.1:p.Ser805Ala
NM_001382806.1:c.2326T>G	NP_001369735.1:p.Ser776Ala
NM_004448.4:c.3364T>G MANE Select	NP_004439.2:p.Ser1122Ala
NR_110535.2:n.3602T>G