Canonical Allele Identifier: CA399312557

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143252200
• MyVariant Identifiers: chr17:g.37883723A>G (hg19) ; chr17:g.39727470A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727470A>G , CM000679.2:g.39727470A>G	GRCh38
NC_000017.10:g.37883723A>G , CM000679.1:g.37883723A>G	GRCh37
NC_000017.9:g.35137249A>G	NCBI36
NG_007503.1:g.44331A>G , LRG_724:g.44331A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3335A>G MANE Select	ENSP00000269571.4:p.Tyr1112Cys
ENST00000269571.9:c.3335A>G	ENSP00000269571.4:p.Tyr1112Cys
ENST00000406381.6:c.3245A>G	ENSP00000385185.2:p.Tyr1082Cys
ENST00000445658.6:c.2507A>G	ENSP00000404047.2:p.Tyr836Cys
ENST00000541774.5:c.3290A>G	ENSP00000446466.1:p.Tyr1097Cys
ENST00000578373.5:c.*3125A>G	ENSP00000463427.1:n.*3125A>G
ENST00000584450.5:c.3160-219A>G	ENSP00000463714.1:n.3160-219A>G
ENST00000584601.5:c.3245A>G	ENSP00000462438.1:p.Tyr1082Cys
NM_001005862.2:c.3245A>G , LRG_724t1:c.3245A>G	NP_001005862.1:p.Tyr1082Cys
NM_001289936.1:c.3290A>G , LRG_724t4:c.3290A>G	NP_001276865.1:p.Tyr1097Cys
NM_001289937.1:c.3160-219A>G	NP_001276866.1:n.3160-219A>G
NM_004448.3:c.3335A>G , LRG_724t2:c.3335A>G	NP_004439.2:p.Tyr1112Cys
NR_110535.1:n.3659A>G
XM_024450641.1:c.3473A>G	XP_024306409.1:p.Tyr1158Cys
XM_024450642.1:c.3428A>G	XP_024306410.1:p.Tyr1143Cys
XM_024450643.1:c.3383A>G	XP_024306411.1:p.Tyr1128Cys
NM_001005862.3:c.3245A>G	NP_001005862.1:p.Tyr1082Cys
NM_001289936.2:c.3290A>G	NP_001276865.1:p.Tyr1097Cys
NM_001289937.2:c.3160-219A>G	NP_001276866.1:n.3160-219A>G
NM_001382782.1:c.3245A>G	NP_001369711.1:p.Tyr1082Cys
NM_001382783.1:c.3245A>G	NP_001369712.1:p.Tyr1082Cys
NM_001382784.1:c.3452A>G	NP_001369713.1:p.Tyr1151Cys
NM_001382785.1:c.3437A>G	NP_001369714.1:p.Tyr1146Cys
NM_001382786.1:c.3416A>G	NP_001369715.1:p.Tyr1139Cys
NM_001382787.1:c.3410A>G	NP_001369716.1:p.Tyr1137Cys
NM_001382788.1:c.3365A>G	NP_001369717.1:p.Tyr1122Cys
NM_001382789.1:c.3356A>G	NP_001369718.1:p.Tyr1119Cys
NM_001382790.1:c.3332A>G	NP_001369719.1:p.Tyr1111Cys
NM_001382791.1:c.3326A>G	NP_001369720.1:p.Tyr1109Cys
NM_001382792.1:c.3299A>G	NP_001369721.1:p.Tyr1100Cys
NM_001382793.1:c.3293A>G	NP_001369722.1:p.Tyr1098Cys
NM_001382794.1:c.3293A>G	NP_001369723.1:p.Tyr1098Cys
NM_001382795.1:c.3287A>G	NP_001369724.1:p.Tyr1096Cys
NM_001382796.1:c.3248A>G	NP_001369725.1:p.Tyr1083Cys
NM_001382797.1:c.3236A>G	NP_001369726.1:p.Tyr1079Cys
NM_001382798.1:c.3179A>G	NP_001369727.1:p.Tyr1060Cys
NM_001382799.1:c.3155A>G	NP_001369728.1:p.Tyr1052Cys
NM_001382800.1:c.3149A>G	NP_001369729.1:p.Tyr1050Cys
NM_001382801.1:c.3131A>G	NP_001369730.1:p.Tyr1044Cys
NM_001382802.1:c.3077A>G	NP_001369731.1:p.Tyr1026Cys
NM_001382803.1:c.3118-219A>G	NP_001369732.1:n.3118-219A>G
NM_001382804.1:c.2507A>G	NP_001369733.1:p.Tyr836Cys
NM_001382805.1:c.2384A>G	NP_001369734.1:p.Tyr795Cys
NM_001382806.1:c.2297A>G	NP_001369735.1:p.Tyr766Cys
NM_004448.4:c.3335A>G MANE Select	NP_004439.2:p.Tyr1112Cys
NR_110535.2:n.3573A>G