Canonical Allele Identifier: CA399304423

Gene: ERBB2

Linked Data

• dbSNP Id: rs2145864015
• MyVariant Identifiers: chr17:g.37881351C>T (hg19) ; chr17:g.39725098C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39725098C>T , CM000679.2:g.39725098C>T	GRCh38
NC_000017.10:g.37881351C>T , CM000679.1:g.37881351C>T	GRCh37
NC_000017.9:g.35134877C>T	NCBI36
NG_007503.1:g.41959C>T , LRG_724:g.41959C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.2543C>T MANE Select	ENSP00000269571.4:p.Ala848Val
ENST00000269571.9:c.2543C>T	ENSP00000269571.4:p.Ala848Val
ENST00000406381.6:c.2453C>T	ENSP00000385185.2:p.Ala818Val
ENST00000445658.6:c.1715C>T	ENSP00000404047.2:p.Ala572Val
ENST00000541774.5:c.2498C>T	ENSP00000446466.1:p.Ala833Val
ENST00000578373.5:c.*2333C>T	ENSP00000463427.1:n.*2333C>T
ENST00000580074.1:c.649C>T
ENST00000583038.5:n.3677C>T
ENST00000584450.5:c.2543C>T	ENSP00000463714.1:p.Ala848Val
ENST00000584601.5:c.2453C>T	ENSP00000462438.1:p.Ala818Val
NM_001005862.2:c.2453C>T , LRG_724t1:c.2453C>T	NP_001005862.1:p.Ala818Val
NM_001289936.1:c.2498C>T , LRG_724t4:c.2498C>T	NP_001276865.1:p.Ala833Val
NM_001289937.1:c.2543C>T	NP_001276866.1:p.Ala848Val
NM_004448.3:c.2543C>T , LRG_724t2:c.2543C>T	NP_004439.2:p.Ala848Val
NR_110535.1:n.2867C>T
XM_024450641.1:c.2681C>T	XP_024306409.1:p.Ala894Val
XM_024450642.1:c.2636C>T	XP_024306410.1:p.Ala879Val
XM_024450643.1:c.2591C>T	XP_024306411.1:p.Ala864Val
NM_001005862.3:c.2453C>T	NP_001005862.1:p.Ala818Val
NM_001289936.2:c.2498C>T	NP_001276865.1:p.Ala833Val
NM_001289937.2:c.2543C>T	NP_001276866.1:p.Ala848Val
NM_001382782.1:c.2453C>T	NP_001369711.1:p.Ala818Val
NM_001382783.1:c.2453C>T	NP_001369712.1:p.Ala818Val
NM_001382784.1:c.2660C>T	NP_001369713.1:p.Ala887Val
NM_001382785.1:c.2645C>T	NP_001369714.1:p.Ala882Val
NM_001382786.1:c.2624C>T	NP_001369715.1:p.Ala875Val
NM_001382787.1:c.2618C>T	NP_001369716.1:p.Ala873Val
NM_001382788.1:c.2573C>T	NP_001369717.1:p.Ala858Val
NM_001382789.1:c.2564C>T	NP_001369718.1:p.Ala855Val
NM_001382790.1:c.2540C>T	NP_001369719.1:p.Ala847Val
NM_001382791.1:c.2534C>T	NP_001369720.1:p.Ala845Val
NM_001382792.1:c.2507C>T	NP_001369721.1:p.Ala836Val
NM_001382793.1:c.2501C>T	NP_001369722.1:p.Ala834Val
NM_001382794.1:c.2501C>T	NP_001369723.1:p.Ala834Val
NM_001382795.1:c.2495C>T	NP_001369724.1:p.Ala832Val
NM_001382796.1:c.2543C>T	NP_001369725.1:p.Ala848Val
NM_001382797.1:c.2444C>T	NP_001369726.1:p.Ala815Val
NM_001382798.1:c.2493+187C>T	NP_001369727.1:n.2493+187C>T
NM_001382799.1:c.2363C>T	NP_001369728.1:p.Ala788Val
NM_001382800.1:c.2357C>T	NP_001369729.1:p.Ala786Val
NM_001382801.1:c.2445+187C>T	NP_001369730.1:n.2445+187C>T
NM_001382802.1:c.2285C>T	NP_001369731.1:p.Ala762Val
NM_001382803.1:c.2501C>T	NP_001369732.1:p.Ala834Val
NM_001382804.1:c.1715C>T	NP_001369733.1:p.Ala572Val
NM_001382805.1:c.2208+1438C>T	NP_001369734.1:n.2208+1438C>T
NM_001382806.1:c.1505C>T	NP_001369735.1:p.Ala502Val
NM_004448.4:c.2543C>T MANE Select	NP_004439.2:p.Ala848Val
NR_110535.2:n.2781C>T