Canonical Allele Identifier: CA399314179

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143311001
• MyVariant Identifiers: chr17:g.37884169A>C (hg19) ; chr17:g.39727916A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727916A>C , CM000679.2:g.39727916A>C	GRCh38
NC_000017.10:g.37884169A>C , CM000679.1:g.37884169A>C	GRCh37
NC_000017.9:g.35137695A>C	NCBI36
NG_007503.1:g.44777A>C , LRG_724:g.44777A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3640A>C MANE Select	ENSP00000269571.4:p.Ser1214Arg
ENST00000269571.9:c.3640A>C	ENSP00000269571.4:p.Ser1214Arg
ENST00000406381.6:c.3550A>C	ENSP00000385185.2:p.Ser1184Arg
ENST00000445658.6:c.2812A>C	ENSP00000404047.2:p.Ser938Arg
ENST00000541774.5:c.3595A>C	ENSP00000446466.1:p.Ser1199Arg
ENST00000578373.5:c.*3430A>C	ENSP00000463427.1:n.*3430A>C
ENST00000584450.5:c.*219A>C	ENSP00000463714.1:n.*219A>C
ENST00000584601.5:c.3550A>C	ENSP00000462438.1:p.Ser1184Arg
NM_001005862.2:c.3550A>C , LRG_724t1:c.3550A>C	NP_001005862.1:p.Ser1184Arg
NM_001289936.1:c.3595A>C , LRG_724t4:c.3595A>C	NP_001276865.1:p.Ser1199Arg
NM_001289937.1:c.*219A>C	NP_001276866.1:n.*219A>C
NM_004448.3:c.3640A>C , LRG_724t2:c.3640A>C	NP_004439.2:p.Ser1214Arg
NR_110535.1:n.3964A>C
XM_024450641.1:c.3778A>C	XP_024306409.1:p.Ser1260Arg
XM_024450642.1:c.3733A>C	XP_024306410.1:p.Ser1245Arg
XM_024450643.1:c.3688A>C	XP_024306411.1:p.Ser1230Arg
NM_001005862.3:c.3550A>C	NP_001005862.1:p.Ser1184Arg
NM_001289936.2:c.3595A>C	NP_001276865.1:p.Ser1199Arg
NM_001289937.2:c.*219A>C	NP_001276866.1:n.*219A>C
NM_001382782.1:c.3550A>C	NP_001369711.1:p.Ser1184Arg
NM_001382783.1:c.3550A>C	NP_001369712.1:p.Ser1184Arg
NM_001382784.1:c.3757A>C	NP_001369713.1:p.Ser1253Arg
NM_001382785.1:c.3742A>C	NP_001369714.1:p.Ser1248Arg
NM_001382786.1:c.3721A>C	NP_001369715.1:p.Ser1241Arg
NM_001382787.1:c.3715A>C	NP_001369716.1:p.Ser1239Arg
NM_001382788.1:c.3670A>C	NP_001369717.1:p.Ser1224Arg
NM_001382789.1:c.3661A>C	NP_001369718.1:p.Ser1221Arg
NM_001382790.1:c.3637A>C	NP_001369719.1:p.Ser1213Arg
NM_001382791.1:c.3631A>C	NP_001369720.1:p.Ser1211Arg
NM_001382792.1:c.3604A>C	NP_001369721.1:p.Ser1202Arg
NM_001382793.1:c.3598A>C	NP_001369722.1:p.Ser1200Arg
NM_001382794.1:c.3598A>C	NP_001369723.1:p.Ser1200Arg
NM_001382795.1:c.3592A>C	NP_001369724.1:p.Ser1198Arg
NM_001382796.1:c.3553A>C	NP_001369725.1:p.Ser1185Arg
NM_001382797.1:c.3541A>C	NP_001369726.1:p.Ser1181Arg
NM_001382798.1:c.3484A>C	NP_001369727.1:p.Ser1162Arg
NM_001382799.1:c.3460A>C	NP_001369728.1:p.Ser1154Arg
NM_001382800.1:c.3454A>C	NP_001369729.1:p.Ser1152Arg
NM_001382801.1:c.3436A>C	NP_001369730.1:p.Ser1146Arg
NM_001382802.1:c.3382A>C	NP_001369731.1:p.Ser1128Arg
NM_001382803.1:c.*219A>C	NP_001369732.1:n.*219A>C
NM_001382804.1:c.2812A>C	NP_001369733.1:p.Ser938Arg
NM_001382805.1:c.2689A>C	NP_001369734.1:p.Ser897Arg
NM_001382806.1:c.2602A>C	NP_001369735.1:p.Ser868Arg
NM_004448.4:c.3640A>C MANE Select	NP_004439.2:p.Ser1214Arg
NR_110535.2:n.3878A>C