Canonical Allele Identifier: CA399312881

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143289277
• MyVariant Identifiers: chr17:g.37883971C>G (hg19) ; chr17:g.39727718C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727718C>G , CM000679.2:g.39727718C>G	GRCh38
NC_000017.10:g.37883971C>G , CM000679.1:g.37883971C>G	GRCh37
NC_000017.9:g.35137497C>G	NCBI36
NG_007503.1:g.44579C>G , LRG_724:g.44579C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3442C>G MANE Select	ENSP00000269571.4:p.Gln1148Glu
ENST00000269571.9:c.3442C>G	ENSP00000269571.4:p.Gln1148Glu
ENST00000406381.6:c.3352C>G	ENSP00000385185.2:p.Gln1118Glu
ENST00000445658.6:c.2614C>G	ENSP00000404047.2:p.Gln872Glu
ENST00000541774.5:c.3397C>G	ENSP00000446466.1:p.Gln1133Glu
ENST00000578373.5:c.*3232C>G	ENSP00000463427.1:n.*3232C>G
ENST00000584450.5:c.*21C>G	ENSP00000463714.1:n.*21C>G
ENST00000584601.5:c.3352C>G	ENSP00000462438.1:p.Gln1118Glu
NM_001005862.2:c.3352C>G , LRG_724t1:c.3352C>G	NP_001005862.1:p.Gln1118Glu
NM_001289936.1:c.3397C>G , LRG_724t4:c.3397C>G	NP_001276865.1:p.Gln1133Glu
NM_001289937.1:c.*21C>G	NP_001276866.1:n.*21C>G
NM_004448.3:c.3442C>G , LRG_724t2:c.3442C>G	NP_004439.2:p.Gln1148Glu
NR_110535.1:n.3766C>G
XM_024450641.1:c.3580C>G	XP_024306409.1:p.Gln1194Glu
XM_024450642.1:c.3535C>G	XP_024306410.1:p.Gln1179Glu
XM_024450643.1:c.3490C>G	XP_024306411.1:p.Gln1164Glu
NM_001005862.3:c.3352C>G	NP_001005862.1:p.Gln1118Glu
NM_001289936.2:c.3397C>G	NP_001276865.1:p.Gln1133Glu
NM_001289937.2:c.*21C>G	NP_001276866.1:n.*21C>G
NM_001382782.1:c.3352C>G	NP_001369711.1:p.Gln1118Glu
NM_001382783.1:c.3352C>G	NP_001369712.1:p.Gln1118Glu
NM_001382784.1:c.3559C>G	NP_001369713.1:p.Gln1187Glu
NM_001382785.1:c.3544C>G	NP_001369714.1:p.Gln1182Glu
NM_001382786.1:c.3523C>G	NP_001369715.1:p.Gln1175Glu
NM_001382787.1:c.3517C>G	NP_001369716.1:p.Gln1173Glu
NM_001382788.1:c.3472C>G	NP_001369717.1:p.Gln1158Glu
NM_001382789.1:c.3463C>G	NP_001369718.1:p.Gln1155Glu
NM_001382790.1:c.3439C>G	NP_001369719.1:p.Gln1147Glu
NM_001382791.1:c.3433C>G	NP_001369720.1:p.Gln1145Glu
NM_001382792.1:c.3406C>G	NP_001369721.1:p.Gln1136Glu
NM_001382793.1:c.3400C>G	NP_001369722.1:p.Gln1134Glu
NM_001382794.1:c.3400C>G	NP_001369723.1:p.Gln1134Glu
NM_001382795.1:c.3394C>G	NP_001369724.1:p.Gln1132Glu
NM_001382796.1:c.3355C>G	NP_001369725.1:p.Gln1119Glu
NM_001382797.1:c.3343C>G	NP_001369726.1:p.Gln1115Glu
NM_001382798.1:c.3286C>G	NP_001369727.1:p.Gln1096Glu
NM_001382799.1:c.3262C>G	NP_001369728.1:p.Gln1088Glu
NM_001382800.1:c.3256C>G	NP_001369729.1:p.Gln1086Glu
NM_001382801.1:c.3238C>G	NP_001369730.1:p.Gln1080Glu
NM_001382802.1:c.3184C>G	NP_001369731.1:p.Gln1062Glu
NM_001382803.1:c.*21C>G	NP_001369732.1:n.*21C>G
NM_001382804.1:c.2614C>G	NP_001369733.1:p.Gln872Glu
NM_001382805.1:c.2491C>G	NP_001369734.1:p.Gln831Glu
NM_001382806.1:c.2404C>G	NP_001369735.1:p.Gln802Glu
NM_004448.4:c.3442C>G MANE Select	NP_004439.2:p.Gln1148Glu
NR_110535.2:n.3680C>G