Canonical Allele Identifier: CA399314590

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143315801
• MyVariant Identifiers: chr17:g.37884221G>C (hg19) ; chr17:g.39727968G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727968G>C , CM000679.2:g.39727968G>C	GRCh38
NC_000017.10:g.37884221G>C , CM000679.1:g.37884221G>C	GRCh37
NC_000017.9:g.35137747G>C	NCBI36
NG_007503.1:g.44829G>C , LRG_724:g.44829G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3692G>C MANE Select	ENSP00000269571.4:p.Gly1231Ala
ENST00000269571.9:c.3692G>C	ENSP00000269571.4:p.Gly1231Ala
ENST00000406381.6:c.3602G>C	ENSP00000385185.2:p.Gly1201Ala
ENST00000445658.6:c.2864G>C	ENSP00000404047.2:p.Gly955Ala
ENST00000541774.5:c.3647G>C	ENSP00000446466.1:p.Gly1216Ala
ENST00000578373.5:c.*3482G>C	ENSP00000463427.1:n.*3482G>C
ENST00000584450.5:c.*271G>C	ENSP00000463714.1:n.*271G>C
ENST00000584601.5:c.3602G>C	ENSP00000462438.1:p.Gly1201Ala
NM_001005862.2:c.3602G>C , LRG_724t1:c.3602G>C	NP_001005862.1:p.Gly1201Ala
NM_001289936.1:c.3647G>C , LRG_724t4:c.3647G>C	NP_001276865.1:p.Gly1216Ala
NM_001289937.1:c.*271G>C	NP_001276866.1:n.*271G>C
NM_004448.3:c.3692G>C , LRG_724t2:c.3692G>C	NP_004439.2:p.Gly1231Ala
NR_110535.1:n.4016G>C
XM_024450641.1:c.3830G>C	XP_024306409.1:p.Gly1277Ala
XM_024450642.1:c.3785G>C	XP_024306410.1:p.Gly1262Ala
XM_024450643.1:c.3740G>C	XP_024306411.1:p.Gly1247Ala
NM_001005862.3:c.3602G>C	NP_001005862.1:p.Gly1201Ala
NM_001289936.2:c.3647G>C	NP_001276865.1:p.Gly1216Ala
NM_001289937.2:c.*271G>C	NP_001276866.1:n.*271G>C
NM_001382782.1:c.3602G>C	NP_001369711.1:p.Gly1201Ala
NM_001382783.1:c.3602G>C	NP_001369712.1:p.Gly1201Ala
NM_001382784.1:c.3809G>C	NP_001369713.1:p.Gly1270Ala
NM_001382785.1:c.3794G>C	NP_001369714.1:p.Gly1265Ala
NM_001382786.1:c.3773G>C	NP_001369715.1:p.Gly1258Ala
NM_001382787.1:c.3767G>C	NP_001369716.1:p.Gly1256Ala
NM_001382788.1:c.3722G>C	NP_001369717.1:p.Gly1241Ala
NM_001382789.1:c.3713G>C	NP_001369718.1:p.Gly1238Ala
NM_001382790.1:c.3689G>C	NP_001369719.1:p.Gly1230Ala
NM_001382791.1:c.3683G>C	NP_001369720.1:p.Gly1228Ala
NM_001382792.1:c.3656G>C	NP_001369721.1:p.Gly1219Ala
NM_001382793.1:c.3650G>C	NP_001369722.1:p.Gly1217Ala
NM_001382794.1:c.3650G>C	NP_001369723.1:p.Gly1217Ala
NM_001382795.1:c.3644G>C	NP_001369724.1:p.Gly1215Ala
NM_001382796.1:c.3605G>C	NP_001369725.1:p.Gly1202Ala
NM_001382797.1:c.3593G>C	NP_001369726.1:p.Gly1198Ala
NM_001382798.1:c.3536G>C	NP_001369727.1:p.Gly1179Ala
NM_001382799.1:c.3512G>C	NP_001369728.1:p.Gly1171Ala
NM_001382800.1:c.3506G>C	NP_001369729.1:p.Gly1169Ala
NM_001382801.1:c.3488G>C	NP_001369730.1:p.Gly1163Ala
NM_001382802.1:c.3434G>C	NP_001369731.1:p.Gly1145Ala
NM_001382803.1:c.*271G>C	NP_001369732.1:n.*271G>C
NM_001382804.1:c.2864G>C	NP_001369733.1:p.Gly955Ala
NM_001382805.1:c.2741G>C	NP_001369734.1:p.Gly914Ala
NM_001382806.1:c.2654G>C	NP_001369735.1:p.Gly885Ala
NM_004448.4:c.3692G>C MANE Select	NP_004439.2:p.Gly1231Ala
NR_110535.2:n.3930G>C