Canonical Allele Identifier: CA499890732

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143301787
• MyVariant Identifiers: chr17:g.37884084T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727831T>C , CM000679.2:g.39727831T>C	GRCh38
NC_000017.10:g.37884084T>C , CM000679.1:g.37884084T>C	GRCh37
NC_000017.9:g.35137610T>C	NCBI36
NG_007503.1:g.44692T>C , LRG_724:g.44692T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3555T>C MANE Select	ENSP00000269571.4:p.Phe1185=
ENST00000269571.9:c.3555T>C	ENSP00000269571.4:p.Phe1185=
ENST00000406381.6:c.3465T>C	ENSP00000385185.2:p.Phe1155=
ENST00000445658.6:c.2727T>C	ENSP00000404047.2:p.Phe909=
ENST00000541774.5:c.3510T>C	ENSP00000446466.1:p.Phe1170=
ENST00000578373.5:c.*3345T>C	ENSP00000463427.1:n.*3345T>C
ENST00000584450.5:c.*134T>C	ENSP00000463714.1:n.*134T>C
ENST00000584601.5:c.3465T>C	ENSP00000462438.1:p.Phe1155=
NM_001005862.2:c.3465T>C , LRG_724t1:c.3465T>C	NP_001005862.1:p.Phe1155=
NM_001289936.1:c.3510T>C , LRG_724t4:c.3510T>C	NP_001276865.1:p.Phe1170=
NM_001289937.1:c.*134T>C	NP_001276866.1:n.*134T>C
NM_004448.3:c.3555T>C , LRG_724t2:c.3555T>C	NP_004439.2:p.Phe1185=
NR_110535.1:n.3879T>C
XM_024450641.1:c.3693T>C	XP_024306409.1:p.Phe1231=
XM_024450642.1:c.3648T>C	XP_024306410.1:p.Phe1216=
XM_024450643.1:c.3603T>C	XP_024306411.1:p.Phe1201=
NM_001005862.3:c.3465T>C	NP_001005862.1:p.Phe1155=
NM_001289936.2:c.3510T>C	NP_001276865.1:p.Phe1170=
NM_001289937.2:c.*134T>C	NP_001276866.1:n.*134T>C
NM_001382782.1:c.3465T>C	NP_001369711.1:p.Phe1155=
NM_001382783.1:c.3465T>C	NP_001369712.1:p.Phe1155=
NM_001382784.1:c.3672T>C	NP_001369713.1:p.Phe1224=
NM_001382785.1:c.3657T>C	NP_001369714.1:p.Phe1219=
NM_001382786.1:c.3636T>C	NP_001369715.1:p.Phe1212=
NM_001382787.1:c.3630T>C	NP_001369716.1:p.Phe1210=
NM_001382788.1:c.3585T>C	NP_001369717.1:p.Phe1195=
NM_001382789.1:c.3576T>C	NP_001369718.1:p.Phe1192=
NM_001382790.1:c.3552T>C	NP_001369719.1:p.Phe1184=
NM_001382791.1:c.3546T>C	NP_001369720.1:p.Phe1182=
NM_001382792.1:c.3519T>C	NP_001369721.1:p.Phe1173=
NM_001382793.1:c.3513T>C	NP_001369722.1:p.Phe1171=
NM_001382794.1:c.3513T>C	NP_001369723.1:p.Phe1171=
NM_001382795.1:c.3507T>C	NP_001369724.1:p.Phe1169=
NM_001382796.1:c.3468T>C	NP_001369725.1:p.Phe1156=
NM_001382797.1:c.3456T>C	NP_001369726.1:p.Phe1152=
NM_001382798.1:c.3399T>C	NP_001369727.1:p.Phe1133=
NM_001382799.1:c.3375T>C	NP_001369728.1:p.Phe1125=
NM_001382800.1:c.3369T>C	NP_001369729.1:p.Phe1123=
NM_001382801.1:c.3351T>C	NP_001369730.1:p.Phe1117=
NM_001382802.1:c.3297T>C	NP_001369731.1:p.Phe1099=
NM_001382803.1:c.*134T>C	NP_001369732.1:n.*134T>C
NM_001382804.1:c.2727T>C	NP_001369733.1:p.Phe909=
NM_001382805.1:c.2604T>C	NP_001369734.1:p.Phe868=
NM_001382806.1:c.2517T>C	NP_001369735.1:p.Phe839=
NM_004448.4:c.3555T>C MANE Select	NP_004439.2:p.Phe1185=
NR_110535.2:n.3793T>C