Canonical Allele Identifier: CA399314135

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143310445
• MyVariant Identifiers: chr17:g.37884163G>C (hg19) ; chr17:g.39727910G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727910G>C , CM000679.2:g.39727910G>C	GRCh38
NC_000017.10:g.37884163G>C , CM000679.1:g.37884163G>C	GRCh37
NC_000017.9:g.35137689G>C	NCBI36
NG_007503.1:g.44771G>C , LRG_724:g.44771G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3634G>C MANE Select	ENSP00000269571.4:p.Ala1212Pro
ENST00000269571.9:c.3634G>C	ENSP00000269571.4:p.Ala1212Pro
ENST00000406381.6:c.3544G>C	ENSP00000385185.2:p.Ala1182Pro
ENST00000445658.6:c.2806G>C	ENSP00000404047.2:p.Ala936Pro
ENST00000541774.5:c.3589G>C	ENSP00000446466.1:p.Ala1197Pro
ENST00000578373.5:c.*3424G>C	ENSP00000463427.1:n.*3424G>C
ENST00000584450.5:c.*213G>C	ENSP00000463714.1:n.*213G>C
ENST00000584601.5:c.3544G>C	ENSP00000462438.1:p.Ala1182Pro
NM_001005862.2:c.3544G>C , LRG_724t1:c.3544G>C	NP_001005862.1:p.Ala1182Pro
NM_001289936.1:c.3589G>C , LRG_724t4:c.3589G>C	NP_001276865.1:p.Ala1197Pro
NM_001289937.1:c.*213G>C	NP_001276866.1:n.*213G>C
NM_004448.3:c.3634G>C , LRG_724t2:c.3634G>C	NP_004439.2:p.Ala1212Pro
NR_110535.1:n.3958G>C
XM_024450641.1:c.3772G>C	XP_024306409.1:p.Ala1258Pro
XM_024450642.1:c.3727G>C	XP_024306410.1:p.Ala1243Pro
XM_024450643.1:c.3682G>C	XP_024306411.1:p.Ala1228Pro
NM_001005862.3:c.3544G>C	NP_001005862.1:p.Ala1182Pro
NM_001289936.2:c.3589G>C	NP_001276865.1:p.Ala1197Pro
NM_001289937.2:c.*213G>C	NP_001276866.1:n.*213G>C
NM_001382782.1:c.3544G>C	NP_001369711.1:p.Ala1182Pro
NM_001382783.1:c.3544G>C	NP_001369712.1:p.Ala1182Pro
NM_001382784.1:c.3751G>C	NP_001369713.1:p.Ala1251Pro
NM_001382785.1:c.3736G>C	NP_001369714.1:p.Ala1246Pro
NM_001382786.1:c.3715G>C	NP_001369715.1:p.Ala1239Pro
NM_001382787.1:c.3709G>C	NP_001369716.1:p.Ala1237Pro
NM_001382788.1:c.3664G>C	NP_001369717.1:p.Ala1222Pro
NM_001382789.1:c.3655G>C	NP_001369718.1:p.Ala1219Pro
NM_001382790.1:c.3631G>C	NP_001369719.1:p.Ala1211Pro
NM_001382791.1:c.3625G>C	NP_001369720.1:p.Ala1209Pro
NM_001382792.1:c.3598G>C	NP_001369721.1:p.Ala1200Pro
NM_001382793.1:c.3592G>C	NP_001369722.1:p.Ala1198Pro
NM_001382794.1:c.3592G>C	NP_001369723.1:p.Ala1198Pro
NM_001382795.1:c.3586G>C	NP_001369724.1:p.Ala1196Pro
NM_001382796.1:c.3547G>C	NP_001369725.1:p.Ala1183Pro
NM_001382797.1:c.3535G>C	NP_001369726.1:p.Ala1179Pro
NM_001382798.1:c.3478G>C	NP_001369727.1:p.Ala1160Pro
NM_001382799.1:c.3454G>C	NP_001369728.1:p.Ala1152Pro
NM_001382800.1:c.3448G>C	NP_001369729.1:p.Ala1150Pro
NM_001382801.1:c.3430G>C	NP_001369730.1:p.Ala1144Pro
NM_001382802.1:c.3376G>C	NP_001369731.1:p.Ala1126Pro
NM_001382803.1:c.*213G>C	NP_001369732.1:n.*213G>C
NM_001382804.1:c.2806G>C	NP_001369733.1:p.Ala936Pro
NM_001382805.1:c.2683G>C	NP_001369734.1:p.Ala895Pro
NM_001382806.1:c.2596G>C	NP_001369735.1:p.Ala866Pro
NM_004448.4:c.3634G>C MANE Select	NP_004439.2:p.Ala1212Pro
NR_110535.2:n.3872G>C