Canonical Allele Identifier: CA399313809

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37884117C>A (hg19) ; chr17:g.39727864C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727864C>A , CM000679.2:g.39727864C>A	GRCh38
NC_000017.10:g.37884117C>A , CM000679.1:g.37884117C>A	GRCh37
NC_000017.9:g.35137643C>A	NCBI36
NG_007503.1:g.44725C>A , LRG_724:g.44725C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3588C>A MANE Select	ENSP00000269571.4:p.Tyr1196Ter
ENST00000269571.9:c.3588C>A	ENSP00000269571.4:p.Tyr1196Ter
ENST00000406381.6:c.3498C>A	ENSP00000385185.2:p.Tyr1166Ter
ENST00000445658.6:c.2760C>A	ENSP00000404047.2:p.Tyr920Ter
ENST00000541774.5:c.3543C>A	ENSP00000446466.1:p.Tyr1181Ter
ENST00000578373.5:c.*3378C>A	ENSP00000463427.1:n.*3378C>A
ENST00000584450.5:c.*167C>A	ENSP00000463714.1:n.*167C>A
ENST00000584601.5:c.3498C>A	ENSP00000462438.1:p.Tyr1166Ter
NM_001005862.2:c.3498C>A , LRG_724t1:c.3498C>A	NP_001005862.1:p.Tyr1166Ter
NM_001289936.1:c.3543C>A , LRG_724t4:c.3543C>A	NP_001276865.1:p.Tyr1181Ter
NM_001289937.1:c.*167C>A	NP_001276866.1:n.*167C>A
NM_004448.3:c.3588C>A , LRG_724t2:c.3588C>A	NP_004439.2:p.Tyr1196Ter
NR_110535.1:n.3912C>A
XM_024450641.1:c.3726C>A	XP_024306409.1:p.Tyr1242Ter
XM_024450642.1:c.3681C>A	XP_024306410.1:p.Tyr1227Ter
XM_024450643.1:c.3636C>A	XP_024306411.1:p.Tyr1212Ter
NM_001005862.3:c.3498C>A	NP_001005862.1:p.Tyr1166Ter
NM_001289936.2:c.3543C>A	NP_001276865.1:p.Tyr1181Ter
NM_001289937.2:c.*167C>A	NP_001276866.1:n.*167C>A
NM_001382782.1:c.3498C>A	NP_001369711.1:p.Tyr1166Ter
NM_001382783.1:c.3498C>A	NP_001369712.1:p.Tyr1166Ter
NM_001382784.1:c.3705C>A	NP_001369713.1:p.Tyr1235Ter
NM_001382785.1:c.3690C>A	NP_001369714.1:p.Tyr1230Ter
NM_001382786.1:c.3669C>A	NP_001369715.1:p.Tyr1223Ter
NM_001382787.1:c.3663C>A	NP_001369716.1:p.Tyr1221Ter
NM_001382788.1:c.3618C>A	NP_001369717.1:p.Tyr1206Ter
NM_001382789.1:c.3609C>A	NP_001369718.1:p.Tyr1203Ter
NM_001382790.1:c.3585C>A	NP_001369719.1:p.Tyr1195Ter
NM_001382791.1:c.3579C>A	NP_001369720.1:p.Tyr1193Ter
NM_001382792.1:c.3552C>A	NP_001369721.1:p.Tyr1184Ter
NM_001382793.1:c.3546C>A	NP_001369722.1:p.Tyr1182Ter
NM_001382794.1:c.3546C>A	NP_001369723.1:p.Tyr1182Ter
NM_001382795.1:c.3540C>A	NP_001369724.1:p.Tyr1180Ter
NM_001382796.1:c.3501C>A	NP_001369725.1:p.Tyr1167Ter
NM_001382797.1:c.3489C>A	NP_001369726.1:p.Tyr1163Ter
NM_001382798.1:c.3432C>A	NP_001369727.1:p.Tyr1144Ter
NM_001382799.1:c.3408C>A	NP_001369728.1:p.Tyr1136Ter
NM_001382800.1:c.3402C>A	NP_001369729.1:p.Tyr1134Ter
NM_001382801.1:c.3384C>A	NP_001369730.1:p.Tyr1128Ter
NM_001382802.1:c.3330C>A	NP_001369731.1:p.Tyr1110Ter
NM_001382803.1:c.*167C>A	NP_001369732.1:n.*167C>A
NM_001382804.1:c.2760C>A	NP_001369733.1:p.Tyr920Ter
NM_001382805.1:c.2637C>A	NP_001369734.1:p.Tyr879Ter
NM_001382806.1:c.2550C>A	NP_001369735.1:p.Tyr850Ter
NM_004448.4:c.3588C>A MANE Select	NP_004439.2:p.Tyr1196Ter
NR_110535.2:n.3826C>A