Canonical Allele Identifier: CA399312521

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143250829
• MyVariant Identifiers: chr17:g.37883711C>G (hg19) ; chr17:g.39727458C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727458C>G , CM000679.2:g.39727458C>G	GRCh38
NC_000017.10:g.37883711C>G , CM000679.1:g.37883711C>G	GRCh37
NC_000017.9:g.35137237C>G	NCBI36
NG_007503.1:g.44319C>G , LRG_724:g.44319C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3323C>G MANE Select	ENSP00000269571.4:p.Pro1108Arg
ENST00000269571.9:c.3323C>G	ENSP00000269571.4:p.Pro1108Arg
ENST00000406381.6:c.3233C>G	ENSP00000385185.2:p.Pro1078Arg
ENST00000445658.6:c.2495C>G	ENSP00000404047.2:p.Pro832Arg
ENST00000541774.5:c.3278C>G	ENSP00000446466.1:p.Pro1093Arg
ENST00000578373.5:c.*3113C>G	ENSP00000463427.1:n.*3113C>G
ENST00000584450.5:c.3160-231C>G	ENSP00000463714.1:n.3160-231C>G
ENST00000584601.5:c.3233C>G	ENSP00000462438.1:p.Pro1078Arg
NM_001005862.2:c.3233C>G , LRG_724t1:c.3233C>G	NP_001005862.1:p.Pro1078Arg
NM_001289936.1:c.3278C>G , LRG_724t4:c.3278C>G	NP_001276865.1:p.Pro1093Arg
NM_001289937.1:c.3160-231C>G	NP_001276866.1:n.3160-231C>G
NM_004448.3:c.3323C>G , LRG_724t2:c.3323C>G	NP_004439.2:p.Pro1108Arg
NR_110535.1:n.3647C>G
XM_024450641.1:c.3461C>G	XP_024306409.1:p.Pro1154Arg
XM_024450642.1:c.3416C>G	XP_024306410.1:p.Pro1139Arg
XM_024450643.1:c.3371C>G	XP_024306411.1:p.Pro1124Arg
NM_001005862.3:c.3233C>G	NP_001005862.1:p.Pro1078Arg
NM_001289936.2:c.3278C>G	NP_001276865.1:p.Pro1093Arg
NM_001289937.2:c.3160-231C>G	NP_001276866.1:n.3160-231C>G
NM_001382782.1:c.3233C>G	NP_001369711.1:p.Pro1078Arg
NM_001382783.1:c.3233C>G	NP_001369712.1:p.Pro1078Arg
NM_001382784.1:c.3440C>G	NP_001369713.1:p.Pro1147Arg
NM_001382785.1:c.3425C>G	NP_001369714.1:p.Pro1142Arg
NM_001382786.1:c.3404C>G	NP_001369715.1:p.Pro1135Arg
NM_001382787.1:c.3398C>G	NP_001369716.1:p.Pro1133Arg
NM_001382788.1:c.3353C>G	NP_001369717.1:p.Pro1118Arg
NM_001382789.1:c.3344C>G	NP_001369718.1:p.Pro1115Arg
NM_001382790.1:c.3320C>G	NP_001369719.1:p.Pro1107Arg
NM_001382791.1:c.3314C>G	NP_001369720.1:p.Pro1105Arg
NM_001382792.1:c.3287C>G	NP_001369721.1:p.Pro1096Arg
NM_001382793.1:c.3281C>G	NP_001369722.1:p.Pro1094Arg
NM_001382794.1:c.3281C>G	NP_001369723.1:p.Pro1094Arg
NM_001382795.1:c.3275C>G	NP_001369724.1:p.Pro1092Arg
NM_001382796.1:c.3236C>G	NP_001369725.1:p.Pro1079Arg
NM_001382797.1:c.3224C>G	NP_001369726.1:p.Pro1075Arg
NM_001382798.1:c.3167C>G	NP_001369727.1:p.Pro1056Arg
NM_001382799.1:c.3143C>G	NP_001369728.1:p.Pro1048Arg
NM_001382800.1:c.3137C>G	NP_001369729.1:p.Pro1046Arg
NM_001382801.1:c.3119C>G	NP_001369730.1:p.Pro1040Arg
NM_001382802.1:c.3065C>G	NP_001369731.1:p.Pro1022Arg
NM_001382803.1:c.3118-231C>G	NP_001369732.1:n.3118-231C>G
NM_001382804.1:c.2495C>G	NP_001369733.1:p.Pro832Arg
NM_001382805.1:c.2372C>G	NP_001369734.1:p.Pro791Arg
NM_001382806.1:c.2285C>G	NP_001369735.1:p.Pro762Arg
NM_004448.4:c.3323C>G MANE Select	NP_004439.2:p.Pro1108Arg
NR_110535.2:n.3561C>G