Canonical Allele Identifier: CA399310988

Gene: ERBB2

Linked Data

• dbSNP Id: rs765660593
• MyVariant Identifiers: chr17:g.37883703C>G (hg19) ; chr17:g.39727450C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727450C>G , CM000679.2:g.39727450C>G	GRCh38
NC_000017.10:g.37883703C>G , CM000679.1:g.37883703C>G	GRCh37
NC_000017.9:g.35137229C>G	NCBI36
NG_007503.1:g.44311C>G , LRG_724:g.44311C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3315C>G MANE Select	ENSP00000269571.4:p.Asp1105Glu
ENST00000269571.9:c.3315C>G	ENSP00000269571.4:p.Asp1105Glu
ENST00000406381.6:c.3225C>G	ENSP00000385185.2:p.Asp1075Glu
ENST00000445658.6:c.2487C>G	ENSP00000404047.2:p.Asp829Glu
ENST00000541774.5:c.3270C>G	ENSP00000446466.1:p.Asp1090Glu
ENST00000578373.5:c.*3105C>G	ENSP00000463427.1:n.*3105C>G
ENST00000584450.5:c.3160-239C>G	ENSP00000463714.1:n.3160-239C>G
ENST00000584601.5:c.3225C>G	ENSP00000462438.1:p.Asp1075Glu
NM_001005862.2:c.3225C>G , LRG_724t1:c.3225C>G	NP_001005862.1:p.Asp1075Glu
NM_001289936.1:c.3270C>G , LRG_724t4:c.3270C>G	NP_001276865.1:p.Asp1090Glu
NM_001289937.1:c.3160-239C>G	NP_001276866.1:n.3160-239C>G
NM_004448.3:c.3315C>G , LRG_724t2:c.3315C>G	NP_004439.2:p.Asp1105Glu
NR_110535.1:n.3639C>G
XM_024450641.1:c.3453C>G	XP_024306409.1:p.Asp1151Glu
XM_024450642.1:c.3408C>G	XP_024306410.1:p.Asp1136Glu
XM_024450643.1:c.3363C>G	XP_024306411.1:p.Asp1121Glu
NM_001005862.3:c.3225C>G	NP_001005862.1:p.Asp1075Glu
NM_001289936.2:c.3270C>G	NP_001276865.1:p.Asp1090Glu
NM_001289937.2:c.3160-239C>G	NP_001276866.1:n.3160-239C>G
NM_001382782.1:c.3225C>G	NP_001369711.1:p.Asp1075Glu
NM_001382783.1:c.3225C>G	NP_001369712.1:p.Asp1075Glu
NM_001382784.1:c.3432C>G	NP_001369713.1:p.Asp1144Glu
NM_001382785.1:c.3417C>G	NP_001369714.1:p.Asp1139Glu
NM_001382786.1:c.3396C>G	NP_001369715.1:p.Asp1132Glu
NM_001382787.1:c.3390C>G	NP_001369716.1:p.Asp1130Glu
NM_001382788.1:c.3345C>G	NP_001369717.1:p.Asp1115Glu
NM_001382789.1:c.3336C>G	NP_001369718.1:p.Asp1112Glu
NM_001382790.1:c.3312C>G	NP_001369719.1:p.Asp1104Glu
NM_001382791.1:c.3306C>G	NP_001369720.1:p.Asp1102Glu
NM_001382792.1:c.3279C>G	NP_001369721.1:p.Asp1093Glu
NM_001382793.1:c.3273C>G	NP_001369722.1:p.Asp1091Glu
NM_001382794.1:c.3273C>G	NP_001369723.1:p.Asp1091Glu
NM_001382795.1:c.3267C>G	NP_001369724.1:p.Asp1089Glu
NM_001382796.1:c.3228C>G	NP_001369725.1:p.Asp1076Glu
NM_001382797.1:c.3216C>G	NP_001369726.1:p.Asp1072Glu
NM_001382798.1:c.3159C>G	NP_001369727.1:p.Asp1053Glu
NM_001382799.1:c.3135C>G	NP_001369728.1:p.Asp1045Glu
NM_001382800.1:c.3129C>G	NP_001369729.1:p.Asp1043Glu
NM_001382801.1:c.3111C>G	NP_001369730.1:p.Asp1037Glu
NM_001382802.1:c.3057C>G	NP_001369731.1:p.Asp1019Glu
NM_001382803.1:c.3118-239C>G	NP_001369732.1:n.3118-239C>G
NM_001382804.1:c.2487C>G	NP_001369733.1:p.Asp829Glu
NM_001382805.1:c.2364C>G	NP_001369734.1:p.Asp788Glu
NM_001382806.1:c.2277C>G	NP_001369735.1:p.Asp759Glu
NM_004448.4:c.3315C>G MANE Select	NP_004439.2:p.Asp1105Glu
NR_110535.2:n.3553C>G