Canonical Allele Identifier: CA399314597

Gene: ERBB2

Linked Data

• dbSNP Id: rs1018067615
• MyVariant Identifiers: chr17:g.37884223G>C (hg19) ; chr17:g.39727970G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727970G>C , CM000679.2:g.39727970G>C	GRCh38
NC_000017.10:g.37884223G>C , CM000679.1:g.37884223G>C	GRCh37
NC_000017.9:g.35137749G>C	NCBI36
NG_007503.1:g.44831G>C , LRG_724:g.44831G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3694G>C MANE Select	ENSP00000269571.4:p.Ala1232Pro
ENST00000269571.9:c.3694G>C	ENSP00000269571.4:p.Ala1232Pro
ENST00000406381.6:c.3604G>C	ENSP00000385185.2:p.Ala1202Pro
ENST00000445658.6:c.2866G>C	ENSP00000404047.2:p.Ala956Pro
ENST00000541774.5:c.3649G>C	ENSP00000446466.1:p.Ala1217Pro
ENST00000578373.5:c.*3484G>C	ENSP00000463427.1:n.*3484G>C
ENST00000584450.5:c.*273G>C	ENSP00000463714.1:n.*273G>C
ENST00000584601.5:c.3604G>C	ENSP00000462438.1:p.Ala1202Pro
NM_001005862.2:c.3604G>C , LRG_724t1:c.3604G>C	NP_001005862.1:p.Ala1202Pro
NM_001289936.1:c.3649G>C , LRG_724t4:c.3649G>C	NP_001276865.1:p.Ala1217Pro
NM_001289937.1:c.*273G>C	NP_001276866.1:n.*273G>C
NM_004448.3:c.3694G>C , LRG_724t2:c.3694G>C	NP_004439.2:p.Ala1232Pro
NR_110535.1:n.4018G>C
XM_024450641.1:c.3832G>C	XP_024306409.1:p.Ala1278Pro
XM_024450642.1:c.3787G>C	XP_024306410.1:p.Ala1263Pro
XM_024450643.1:c.3742G>C	XP_024306411.1:p.Ala1248Pro
NM_001005862.3:c.3604G>C	NP_001005862.1:p.Ala1202Pro
NM_001289936.2:c.3649G>C	NP_001276865.1:p.Ala1217Pro
NM_001289937.2:c.*273G>C	NP_001276866.1:n.*273G>C
NM_001382782.1:c.3604G>C	NP_001369711.1:p.Ala1202Pro
NM_001382783.1:c.3604G>C	NP_001369712.1:p.Ala1202Pro
NM_001382784.1:c.3811G>C	NP_001369713.1:p.Ala1271Pro
NM_001382785.1:c.3796G>C	NP_001369714.1:p.Ala1266Pro
NM_001382786.1:c.3775G>C	NP_001369715.1:p.Ala1259Pro
NM_001382787.1:c.3769G>C	NP_001369716.1:p.Ala1257Pro
NM_001382788.1:c.3724G>C	NP_001369717.1:p.Ala1242Pro
NM_001382789.1:c.3715G>C	NP_001369718.1:p.Ala1239Pro
NM_001382790.1:c.3691G>C	NP_001369719.1:p.Ala1231Pro
NM_001382791.1:c.3685G>C	NP_001369720.1:p.Ala1229Pro
NM_001382792.1:c.3658G>C	NP_001369721.1:p.Ala1220Pro
NM_001382793.1:c.3652G>C	NP_001369722.1:p.Ala1218Pro
NM_001382794.1:c.3652G>C	NP_001369723.1:p.Ala1218Pro
NM_001382795.1:c.3646G>C	NP_001369724.1:p.Ala1216Pro
NM_001382796.1:c.3607G>C	NP_001369725.1:p.Ala1203Pro
NM_001382797.1:c.3595G>C	NP_001369726.1:p.Ala1199Pro
NM_001382798.1:c.3538G>C	NP_001369727.1:p.Ala1180Pro
NM_001382799.1:c.3514G>C	NP_001369728.1:p.Ala1172Pro
NM_001382800.1:c.3508G>C	NP_001369729.1:p.Ala1170Pro
NM_001382801.1:c.3490G>C	NP_001369730.1:p.Ala1164Pro
NM_001382802.1:c.3436G>C	NP_001369731.1:p.Ala1146Pro
NM_001382803.1:c.*273G>C	NP_001369732.1:n.*273G>C
NM_001382804.1:c.2866G>C	NP_001369733.1:p.Ala956Pro
NM_001382805.1:c.2743G>C	NP_001369734.1:p.Ala915Pro
NM_001382806.1:c.2656G>C	NP_001369735.1:p.Ala886Pro
NM_004448.4:c.3694G>C MANE Select	NP_004439.2:p.Ala1232Pro
NR_110535.2:n.3932G>C