Canonical Allele Identifier: CA399314601

Gene: ERBB2

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3694G>T MANE Select	ENSP00000269571.4:p.Ala1232Ser
ENST00000269571.9:c.3694G>T	ENSP00000269571.4:p.Ala1232Ser
ENST00000406381.6:c.3604G>T	ENSP00000385185.2:p.Ala1202Ser
ENST00000445658.6:c.2866G>T	ENSP00000404047.2:p.Ala956Ser
ENST00000541774.5:c.3649G>T	ENSP00000446466.1:p.Ala1217Ser
ENST00000578373.5:c.*3484G>T	ENSP00000463427.1:n.*3484G>T
ENST00000584450.5:c.*273G>T	ENSP00000463714.1:n.*273G>T
ENST00000584601.5:c.3604G>T	ENSP00000462438.1:p.Ala1202Ser
NM_001005862.2:c.3604G>T , LRG_724t1:c.3604G>T	NP_001005862.1:p.Ala1202Ser
NM_001289936.1:c.3649G>T , LRG_724t4:c.3649G>T	NP_001276865.1:p.Ala1217Ser
NM_001289937.1:c.*273G>T	NP_001276866.1:n.*273G>T
NM_004448.3:c.3694G>T , LRG_724t2:c.3694G>T	NP_004439.2:p.Ala1232Ser
NR_110535.1:n.4018G>T
XM_024450641.1:c.3832G>T	XP_024306409.1:p.Ala1278Ser
XM_024450642.1:c.3787G>T	XP_024306410.1:p.Ala1263Ser
XM_024450643.1:c.3742G>T	XP_024306411.1:p.Ala1248Ser
NM_001005862.3:c.3604G>T	NP_001005862.1:p.Ala1202Ser
NM_001289936.2:c.3649G>T	NP_001276865.1:p.Ala1217Ser
NM_001289937.2:c.*273G>T	NP_001276866.1:n.*273G>T
NM_001382782.1:c.3604G>T	NP_001369711.1:p.Ala1202Ser
NM_001382783.1:c.3604G>T	NP_001369712.1:p.Ala1202Ser
NM_001382784.1:c.3811G>T	NP_001369713.1:p.Ala1271Ser
NM_001382785.1:c.3796G>T	NP_001369714.1:p.Ala1266Ser
NM_001382786.1:c.3775G>T	NP_001369715.1:p.Ala1259Ser
NM_001382787.1:c.3769G>T	NP_001369716.1:p.Ala1257Ser
NM_001382788.1:c.3724G>T	NP_001369717.1:p.Ala1242Ser
NM_001382789.1:c.3715G>T	NP_001369718.1:p.Ala1239Ser
NM_001382790.1:c.3691G>T	NP_001369719.1:p.Ala1231Ser
NM_001382791.1:c.3685G>T	NP_001369720.1:p.Ala1229Ser
NM_001382792.1:c.3658G>T	NP_001369721.1:p.Ala1220Ser
NM_001382793.1:c.3652G>T	NP_001369722.1:p.Ala1218Ser
NM_001382794.1:c.3652G>T	NP_001369723.1:p.Ala1218Ser
NM_001382795.1:c.3646G>T	NP_001369724.1:p.Ala1216Ser
NM_001382796.1:c.3607G>T	NP_001369725.1:p.Ala1203Ser
NM_001382797.1:c.3595G>T	NP_001369726.1:p.Ala1199Ser
NM_001382798.1:c.3538G>T	NP_001369727.1:p.Ala1180Ser
NM_001382799.1:c.3514G>T	NP_001369728.1:p.Ala1172Ser
NM_001382800.1:c.3508G>T	NP_001369729.1:p.Ala1170Ser
NM_001382801.1:c.3490G>T	NP_001369730.1:p.Ala1164Ser
NM_001382802.1:c.3436G>T	NP_001369731.1:p.Ala1146Ser
NM_001382803.1:c.*273G>T	NP_001369732.1:n.*273G>T
NM_001382804.1:c.2866G>T	NP_001369733.1:p.Ala956Ser
NM_001382805.1:c.2743G>T	NP_001369734.1:p.Ala915Ser
NM_001382806.1:c.2656G>T	NP_001369735.1:p.Ala886Ser
NM_004448.4:c.3694G>T MANE Select	NP_004439.2:p.Ala1232Ser
NR_110535.2:n.3932G>T