Canonical Allele Identifier: CA399313787

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143305114
• MyVariant Identifiers: chr17:g.37884115T>G (hg19) ; chr17:g.39727862T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727862T>G , CM000679.2:g.39727862T>G	GRCh38
NC_000017.10:g.37884115T>G , CM000679.1:g.37884115T>G	GRCh37
NC_000017.9:g.35137641T>G	NCBI36
NG_007503.1:g.44723T>G , LRG_724:g.44723T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3586T>G MANE Select	ENSP00000269571.4:p.Tyr1196Asp
ENST00000269571.9:c.3586T>G	ENSP00000269571.4:p.Tyr1196Asp
ENST00000406381.6:c.3496T>G	ENSP00000385185.2:p.Tyr1166Asp
ENST00000445658.6:c.2758T>G	ENSP00000404047.2:p.Tyr920Asp
ENST00000541774.5:c.3541T>G	ENSP00000446466.1:p.Tyr1181Asp
ENST00000578373.5:c.*3376T>G	ENSP00000463427.1:n.*3376T>G
ENST00000584450.5:c.*165T>G	ENSP00000463714.1:n.*165T>G
ENST00000584601.5:c.3496T>G	ENSP00000462438.1:p.Tyr1166Asp
NM_001005862.2:c.3496T>G , LRG_724t1:c.3496T>G	NP_001005862.1:p.Tyr1166Asp
NM_001289936.1:c.3541T>G , LRG_724t4:c.3541T>G	NP_001276865.1:p.Tyr1181Asp
NM_001289937.1:c.*165T>G	NP_001276866.1:n.*165T>G
NM_004448.3:c.3586T>G , LRG_724t2:c.3586T>G	NP_004439.2:p.Tyr1196Asp
NR_110535.1:n.3910T>G
XM_024450641.1:c.3724T>G	XP_024306409.1:p.Tyr1242Asp
XM_024450642.1:c.3679T>G	XP_024306410.1:p.Tyr1227Asp
XM_024450643.1:c.3634T>G	XP_024306411.1:p.Tyr1212Asp
NM_001005862.3:c.3496T>G	NP_001005862.1:p.Tyr1166Asp
NM_001289936.2:c.3541T>G	NP_001276865.1:p.Tyr1181Asp
NM_001289937.2:c.*165T>G	NP_001276866.1:n.*165T>G
NM_001382782.1:c.3496T>G	NP_001369711.1:p.Tyr1166Asp
NM_001382783.1:c.3496T>G	NP_001369712.1:p.Tyr1166Asp
NM_001382784.1:c.3703T>G	NP_001369713.1:p.Tyr1235Asp
NM_001382785.1:c.3688T>G	NP_001369714.1:p.Tyr1230Asp
NM_001382786.1:c.3667T>G	NP_001369715.1:p.Tyr1223Asp
NM_001382787.1:c.3661T>G	NP_001369716.1:p.Tyr1221Asp
NM_001382788.1:c.3616T>G	NP_001369717.1:p.Tyr1206Asp
NM_001382789.1:c.3607T>G	NP_001369718.1:p.Tyr1203Asp
NM_001382790.1:c.3583T>G	NP_001369719.1:p.Tyr1195Asp
NM_001382791.1:c.3577T>G	NP_001369720.1:p.Tyr1193Asp
NM_001382792.1:c.3550T>G	NP_001369721.1:p.Tyr1184Asp
NM_001382793.1:c.3544T>G	NP_001369722.1:p.Tyr1182Asp
NM_001382794.1:c.3544T>G	NP_001369723.1:p.Tyr1182Asp
NM_001382795.1:c.3538T>G	NP_001369724.1:p.Tyr1180Asp
NM_001382796.1:c.3499T>G	NP_001369725.1:p.Tyr1167Asp
NM_001382797.1:c.3487T>G	NP_001369726.1:p.Tyr1163Asp
NM_001382798.1:c.3430T>G	NP_001369727.1:p.Tyr1144Asp
NM_001382799.1:c.3406T>G	NP_001369728.1:p.Tyr1136Asp
NM_001382800.1:c.3400T>G	NP_001369729.1:p.Tyr1134Asp
NM_001382801.1:c.3382T>G	NP_001369730.1:p.Tyr1128Asp
NM_001382802.1:c.3328T>G	NP_001369731.1:p.Tyr1110Asp
NM_001382803.1:c.*165T>G	NP_001369732.1:n.*165T>G
NM_001382804.1:c.2758T>G	NP_001369733.1:p.Tyr920Asp
NM_001382805.1:c.2635T>G	NP_001369734.1:p.Tyr879Asp
NM_001382806.1:c.2548T>G	NP_001369735.1:p.Tyr850Asp
NM_004448.4:c.3586T>G MANE Select	NP_004439.2:p.Tyr1196Asp
NR_110535.2:n.3824T>G