Canonical Allele Identifier: CA399310334

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143238185
• MyVariant Identifiers: chr17:g.37883605T>A (hg19) ; chr17:g.39727352T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727352T>A , CM000679.2:g.39727352T>A	GRCh38
NC_000017.10:g.37883605T>A , CM000679.1:g.37883605T>A	GRCh37
NC_000017.9:g.35137131T>A	NCBI36
NG_007503.1:g.44213T>A , LRG_724:g.44213T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3217T>A MANE Select	ENSP00000269571.4:p.Ser1073Thr
ENST00000269571.9:c.3217T>A	ENSP00000269571.4:p.Ser1073Thr
ENST00000406381.6:c.3127T>A	ENSP00000385185.2:p.Ser1043Thr
ENST00000445658.6:c.2389T>A	ENSP00000404047.2:p.Ser797Thr
ENST00000541774.5:c.3172T>A	ENSP00000446466.1:p.Ser1058Thr
ENST00000578373.5:c.*3007T>A	ENSP00000463427.1:n.*3007T>A
ENST00000584450.5:c.3160-337T>A	ENSP00000463714.1:n.3160-337T>A
ENST00000584601.5:c.3127T>A	ENSP00000462438.1:p.Ser1043Thr
NM_001005862.2:c.3127T>A , LRG_724t1:c.3127T>A	NP_001005862.1:p.Ser1043Thr
NM_001289936.1:c.3172T>A , LRG_724t4:c.3172T>A	NP_001276865.1:p.Ser1058Thr
NM_001289937.1:c.3160-337T>A	NP_001276866.1:n.3160-337T>A
NM_004448.3:c.3217T>A , LRG_724t2:c.3217T>A	NP_004439.2:p.Ser1073Thr
NR_110535.1:n.3541T>A
XM_024450641.1:c.3355T>A	XP_024306409.1:p.Ser1119Thr
XM_024450642.1:c.3310T>A	XP_024306410.1:p.Ser1104Thr
XM_024450643.1:c.3265T>A	XP_024306411.1:p.Ser1089Thr
NM_001005862.3:c.3127T>A	NP_001005862.1:p.Ser1043Thr
NM_001289936.2:c.3172T>A	NP_001276865.1:p.Ser1058Thr
NM_001289937.2:c.3160-337T>A	NP_001276866.1:n.3160-337T>A
NM_001382782.1:c.3127T>A	NP_001369711.1:p.Ser1043Thr
NM_001382783.1:c.3127T>A	NP_001369712.1:p.Ser1043Thr
NM_001382784.1:c.3334T>A	NP_001369713.1:p.Ser1112Thr
NM_001382785.1:c.3319T>A	NP_001369714.1:p.Ser1107Thr
NM_001382786.1:c.3298T>A	NP_001369715.1:p.Ser1100Thr
NM_001382787.1:c.3292T>A	NP_001369716.1:p.Ser1098Thr
NM_001382788.1:c.3247T>A	NP_001369717.1:p.Ser1083Thr
NM_001382789.1:c.3238T>A	NP_001369718.1:p.Ser1080Thr
NM_001382790.1:c.3214T>A	NP_001369719.1:p.Ser1072Thr
NM_001382791.1:c.3208T>A	NP_001369720.1:p.Ser1070Thr
NM_001382792.1:c.3181T>A	NP_001369721.1:p.Ser1061Thr
NM_001382793.1:c.3175T>A	NP_001369722.1:p.Ser1059Thr
NM_001382794.1:c.3175T>A	NP_001369723.1:p.Ser1059Thr
NM_001382795.1:c.3169T>A	NP_001369724.1:p.Ser1057Thr
NM_001382796.1:c.3130T>A	NP_001369725.1:p.Ser1044Thr
NM_001382797.1:c.3118T>A	NP_001369726.1:p.Ser1040Thr
NM_001382798.1:c.3061T>A	NP_001369727.1:p.Ser1021Thr
NM_001382799.1:c.3037T>A	NP_001369728.1:p.Ser1013Thr
NM_001382800.1:c.3031T>A	NP_001369729.1:p.Ser1011Thr
NM_001382801.1:c.3013T>A	NP_001369730.1:p.Ser1005Thr
NM_001382802.1:c.2959T>A	NP_001369731.1:p.Ser987Thr
NM_001382803.1:c.3118-337T>A	NP_001369732.1:n.3118-337T>A
NM_001382804.1:c.2389T>A	NP_001369733.1:p.Ser797Thr
NM_001382805.1:c.2266T>A	NP_001369734.1:p.Ser756Thr
NM_001382806.1:c.2179T>A	NP_001369735.1:p.Ser727Thr
NM_004448.4:c.3217T>A MANE Select	NP_004439.2:p.Ser1073Thr
NR_110535.2:n.3455T>A