Canonical Allele Identifier: CA499890767

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37884117C>T (hg19)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3588C>T MANE Select	ENSP00000269571.4:p.Tyr1196=
ENST00000269571.9:c.3588C>T	ENSP00000269571.4:p.Tyr1196=
ENST00000406381.6:c.3498C>T	ENSP00000385185.2:p.Tyr1166=
ENST00000445658.6:c.2760C>T	ENSP00000404047.2:p.Tyr920=
ENST00000541774.5:c.3543C>T	ENSP00000446466.1:p.Tyr1181=
ENST00000578373.5:c.*3378C>T	ENSP00000463427.1:n.*3378C>T
ENST00000584450.5:c.*167C>T	ENSP00000463714.1:n.*167C>T
ENST00000584601.5:c.3498C>T	ENSP00000462438.1:p.Tyr1166=
NM_001005862.2:c.3498C>T , LRG_724t1:c.3498C>T	NP_001005862.1:p.Tyr1166=
NM_001289936.1:c.3543C>T , LRG_724t4:c.3543C>T	NP_001276865.1:p.Tyr1181=
NM_001289937.1:c.*167C>T	NP_001276866.1:n.*167C>T
NM_004448.3:c.3588C>T , LRG_724t2:c.3588C>T	NP_004439.2:p.Tyr1196=
NR_110535.1:n.3912C>T
XM_024450641.1:c.3726C>T	XP_024306409.1:p.Tyr1242=
XM_024450642.1:c.3681C>T	XP_024306410.1:p.Tyr1227=
XM_024450643.1:c.3636C>T	XP_024306411.1:p.Tyr1212=
NM_001005862.3:c.3498C>T	NP_001005862.1:p.Tyr1166=
NM_001289936.2:c.3543C>T	NP_001276865.1:p.Tyr1181=
NM_001289937.2:c.*167C>T	NP_001276866.1:n.*167C>T
NM_001382782.1:c.3498C>T	NP_001369711.1:p.Tyr1166=
NM_001382783.1:c.3498C>T	NP_001369712.1:p.Tyr1166=
NM_001382784.1:c.3705C>T	NP_001369713.1:p.Tyr1235=
NM_001382785.1:c.3690C>T	NP_001369714.1:p.Tyr1230=
NM_001382786.1:c.3669C>T	NP_001369715.1:p.Tyr1223=
NM_001382787.1:c.3663C>T	NP_001369716.1:p.Tyr1221=
NM_001382788.1:c.3618C>T	NP_001369717.1:p.Tyr1206=
NM_001382789.1:c.3609C>T	NP_001369718.1:p.Tyr1203=
NM_001382790.1:c.3585C>T	NP_001369719.1:p.Tyr1195=
NM_001382791.1:c.3579C>T	NP_001369720.1:p.Tyr1193=
NM_001382792.1:c.3552C>T	NP_001369721.1:p.Tyr1184=
NM_001382793.1:c.3546C>T	NP_001369722.1:p.Tyr1182=
NM_001382794.1:c.3546C>T	NP_001369723.1:p.Tyr1182=
NM_001382795.1:c.3540C>T	NP_001369724.1:p.Tyr1180=
NM_001382796.1:c.3501C>T	NP_001369725.1:p.Tyr1167=
NM_001382797.1:c.3489C>T	NP_001369726.1:p.Tyr1163=
NM_001382798.1:c.3432C>T	NP_001369727.1:p.Tyr1144=
NM_001382799.1:c.3408C>T	NP_001369728.1:p.Tyr1136=
NM_001382800.1:c.3402C>T	NP_001369729.1:p.Tyr1134=
NM_001382801.1:c.3384C>T	NP_001369730.1:p.Tyr1128=
NM_001382802.1:c.3330C>T	NP_001369731.1:p.Tyr1110=
NM_001382803.1:c.*167C>T	NP_001369732.1:n.*167C>T
NM_001382804.1:c.2760C>T	NP_001369733.1:p.Tyr920=
NM_001382805.1:c.2637C>T	NP_001369734.1:p.Tyr879=
NM_001382806.1:c.2550C>T	NP_001369735.1:p.Tyr850=
NM_004448.4:c.3588C>T MANE Select	NP_004439.2:p.Tyr1196=
NR_110535.2:n.3826C>T