Canonical Allele Identifier: CA399302881

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37881007C>A (hg19) ; chr17:g.39724754C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39724754C>A , CM000679.2:g.39724754C>A	GRCh38
NC_000017.10:g.37881007C>A , CM000679.1:g.37881007C>A	GRCh37
NC_000017.9:g.35134533C>A	NCBI36
NG_007503.1:g.41615C>A , LRG_724:g.41615C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.2336C>A MANE Select	ENSP00000269571.4:p.Ser779Tyr
ENST00000269571.9:c.2336C>A	ENSP00000269571.4:p.Ser779Tyr
ENST00000406381.6:c.2246C>A	ENSP00000385185.2:p.Ser749Tyr
ENST00000445658.6:c.1508C>A	ENSP00000404047.2:p.Ser503Tyr
ENST00000541774.5:c.2291C>A	ENSP00000446466.1:p.Ser764Tyr
ENST00000578373.5:c.*2126C>A	ENSP00000463427.1:n.*2126C>A
ENST00000580074.1:c.442C>A
ENST00000583038.5:n.3470C>A
ENST00000584450.5:c.2336C>A	ENSP00000463714.1:p.Ser779Tyr
ENST00000584601.5:c.2246C>A	ENSP00000462438.1:p.Ser749Tyr
NM_001005862.2:c.2246C>A , LRG_724t1:c.2246C>A	NP_001005862.1:p.Ser749Tyr
NM_001289936.1:c.2291C>A , LRG_724t4:c.2291C>A	NP_001276865.1:p.Ser764Tyr
NM_001289937.1:c.2336C>A	NP_001276866.1:p.Ser779Tyr
NM_004448.3:c.2336C>A , LRG_724t2:c.2336C>A	NP_004439.2:p.Ser779Tyr
NR_110535.1:n.2660C>A
XM_024450641.1:c.2474C>A	XP_024306409.1:p.Ser825Tyr
XM_024450642.1:c.2429C>A	XP_024306410.1:p.Ser810Tyr
XM_024450643.1:c.2384C>A	XP_024306411.1:p.Ser795Tyr
NM_001005862.3:c.2246C>A	NP_001005862.1:p.Ser749Tyr
NM_001289936.2:c.2291C>A	NP_001276865.1:p.Ser764Tyr
NM_001289937.2:c.2336C>A	NP_001276866.1:p.Ser779Tyr
NM_001382782.1:c.2246C>A	NP_001369711.1:p.Ser749Tyr
NM_001382783.1:c.2246C>A	NP_001369712.1:p.Ser749Tyr
NM_001382784.1:c.2453C>A	NP_001369713.1:p.Ser818Tyr
NM_001382785.1:c.2438C>A	NP_001369714.1:p.Ser813Tyr
NM_001382786.1:c.2417C>A	NP_001369715.1:p.Ser806Tyr
NM_001382787.1:c.2411C>A	NP_001369716.1:p.Ser804Tyr
NM_001382788.1:c.2366C>A	NP_001369717.1:p.Ser789Tyr
NM_001382789.1:c.2357C>A	NP_001369718.1:p.Ser786Tyr
NM_001382790.1:c.2333C>A	NP_001369719.1:p.Ser778Tyr
NM_001382791.1:c.2327C>A	NP_001369720.1:p.Ser776Tyr
NM_001382792.1:c.2300C>A	NP_001369721.1:p.Ser767Tyr
NM_001382793.1:c.2294C>A	NP_001369722.1:p.Ser765Tyr
NM_001382794.1:c.2294C>A	NP_001369723.1:p.Ser765Tyr
NM_001382795.1:c.2288C>A	NP_001369724.1:p.Ser763Tyr
NM_001382796.1:c.2336C>A	NP_001369725.1:p.Ser779Tyr
NM_001382797.1:c.2237C>A	NP_001369726.1:p.Ser746Tyr
NM_001382798.1:c.2336C>A	NP_001369727.1:p.Ser779Tyr
NM_001382799.1:c.2156C>A	NP_001369728.1:p.Ser719Tyr
NM_001382800.1:c.2308-295C>A	NP_001369729.1:n.2308-295C>A
NM_001382801.1:c.2288C>A	NP_001369730.1:p.Ser763Tyr
NM_001382802.1:c.2078C>A	NP_001369731.1:p.Ser693Tyr
NM_001382803.1:c.2294C>A	NP_001369732.1:p.Ser765Tyr
NM_001382804.1:c.1508C>A	NP_001369733.1:p.Ser503Tyr
NM_001382805.1:c.2208+1094C>A	NP_001369734.1:n.2208+1094C>A
NM_001382806.1:c.1298C>A	NP_001369735.1:p.Ser433Tyr
NM_004448.4:c.2336C>A MANE Select	NP_004439.2:p.Ser779Tyr
NR_110535.2:n.2574C>A