Canonical Allele Identifier: CA399312555

Gene: ERBB2

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3335A>C MANE Select	ENSP00000269571.4:p.Tyr1112Ser
ENST00000269571.9:c.3335A>C	ENSP00000269571.4:p.Tyr1112Ser
ENST00000406381.6:c.3245A>C	ENSP00000385185.2:p.Tyr1082Ser
ENST00000445658.6:c.2507A>C	ENSP00000404047.2:p.Tyr836Ser
ENST00000541774.5:c.3290A>C	ENSP00000446466.1:p.Tyr1097Ser
ENST00000578373.5:c.*3125A>C	ENSP00000463427.1:n.*3125A>C
ENST00000584450.5:c.3160-219A>C	ENSP00000463714.1:n.3160-219A>C
ENST00000584601.5:c.3245A>C	ENSP00000462438.1:p.Tyr1082Ser
NM_001005862.2:c.3245A>C , LRG_724t1:c.3245A>C	NP_001005862.1:p.Tyr1082Ser
NM_001289936.1:c.3290A>C , LRG_724t4:c.3290A>C	NP_001276865.1:p.Tyr1097Ser
NM_001289937.1:c.3160-219A>C	NP_001276866.1:n.3160-219A>C
NM_004448.3:c.3335A>C , LRG_724t2:c.3335A>C	NP_004439.2:p.Tyr1112Ser
NR_110535.1:n.3659A>C
XM_024450641.1:c.3473A>C	XP_024306409.1:p.Tyr1158Ser
XM_024450642.1:c.3428A>C	XP_024306410.1:p.Tyr1143Ser
XM_024450643.1:c.3383A>C	XP_024306411.1:p.Tyr1128Ser
NM_001005862.3:c.3245A>C	NP_001005862.1:p.Tyr1082Ser
NM_001289936.2:c.3290A>C	NP_001276865.1:p.Tyr1097Ser
NM_001289937.2:c.3160-219A>C	NP_001276866.1:n.3160-219A>C
NM_001382782.1:c.3245A>C	NP_001369711.1:p.Tyr1082Ser
NM_001382783.1:c.3245A>C	NP_001369712.1:p.Tyr1082Ser
NM_001382784.1:c.3452A>C	NP_001369713.1:p.Tyr1151Ser
NM_001382785.1:c.3437A>C	NP_001369714.1:p.Tyr1146Ser
NM_001382786.1:c.3416A>C	NP_001369715.1:p.Tyr1139Ser
NM_001382787.1:c.3410A>C	NP_001369716.1:p.Tyr1137Ser
NM_001382788.1:c.3365A>C	NP_001369717.1:p.Tyr1122Ser
NM_001382789.1:c.3356A>C	NP_001369718.1:p.Tyr1119Ser
NM_001382790.1:c.3332A>C	NP_001369719.1:p.Tyr1111Ser
NM_001382791.1:c.3326A>C	NP_001369720.1:p.Tyr1109Ser
NM_001382792.1:c.3299A>C	NP_001369721.1:p.Tyr1100Ser
NM_001382793.1:c.3293A>C	NP_001369722.1:p.Tyr1098Ser
NM_001382794.1:c.3293A>C	NP_001369723.1:p.Tyr1098Ser
NM_001382795.1:c.3287A>C	NP_001369724.1:p.Tyr1096Ser
NM_001382796.1:c.3248A>C	NP_001369725.1:p.Tyr1083Ser
NM_001382797.1:c.3236A>C	NP_001369726.1:p.Tyr1079Ser
NM_001382798.1:c.3179A>C	NP_001369727.1:p.Tyr1060Ser
NM_001382799.1:c.3155A>C	NP_001369728.1:p.Tyr1052Ser
NM_001382800.1:c.3149A>C	NP_001369729.1:p.Tyr1050Ser
NM_001382801.1:c.3131A>C	NP_001369730.1:p.Tyr1044Ser
NM_001382802.1:c.3077A>C	NP_001369731.1:p.Tyr1026Ser
NM_001382803.1:c.3118-219A>C	NP_001369732.1:n.3118-219A>C
NM_001382804.1:c.2507A>C	NP_001369733.1:p.Tyr836Ser
NM_001382805.1:c.2384A>C	NP_001369734.1:p.Tyr795Ser
NM_001382806.1:c.2297A>C	NP_001369735.1:p.Tyr766Ser
NM_004448.4:c.3335A>C MANE Select	NP_004439.2:p.Tyr1112Ser
NR_110535.2:n.3573A>C