Canonical Allele Identifier: CA399304090

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37881311T>C (hg19) ; chr17:g.39725058T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39725058T>C , CM000679.2:g.39725058T>C	GRCh38
NC_000017.10:g.37881311T>C , CM000679.1:g.37881311T>C	GRCh37
NC_000017.9:g.35134837T>C	NCBI36
NG_007503.1:g.41919T>C , LRG_724:g.41919T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.2503T>C MANE Select	ENSP00000269571.4:p.Tyr835His
ENST00000269571.9:c.2503T>C	ENSP00000269571.4:p.Tyr835His
ENST00000406381.6:c.2413T>C	ENSP00000385185.2:p.Tyr805His
ENST00000445658.6:c.1675T>C	ENSP00000404047.2:p.Tyr559His
ENST00000541774.5:c.2458T>C	ENSP00000446466.1:p.Tyr820His
ENST00000578373.5:c.*2293T>C	ENSP00000463427.1:n.*2293T>C
ENST00000580074.1:c.609T>C
ENST00000583038.5:n.3637T>C
ENST00000584450.5:c.2503T>C	ENSP00000463714.1:p.Tyr835His
ENST00000584601.5:c.2413T>C	ENSP00000462438.1:p.Tyr805His
NM_001005862.2:c.2413T>C , LRG_724t1:c.2413T>C	NP_001005862.1:p.Tyr805His
NM_001289936.1:c.2458T>C , LRG_724t4:c.2458T>C	NP_001276865.1:p.Tyr820His
NM_001289937.1:c.2503T>C	NP_001276866.1:p.Tyr835His
NM_004448.3:c.2503T>C , LRG_724t2:c.2503T>C	NP_004439.2:p.Tyr835His
NR_110535.1:n.2827T>C
XM_024450641.1:c.2641T>C	XP_024306409.1:p.Tyr881His
XM_024450642.1:c.2596T>C	XP_024306410.1:p.Tyr866His
XM_024450643.1:c.2551T>C	XP_024306411.1:p.Tyr851His
NM_001005862.3:c.2413T>C	NP_001005862.1:p.Tyr805His
NM_001289936.2:c.2458T>C	NP_001276865.1:p.Tyr820His
NM_001289937.2:c.2503T>C	NP_001276866.1:p.Tyr835His
NM_001382782.1:c.2413T>C	NP_001369711.1:p.Tyr805His
NM_001382783.1:c.2413T>C	NP_001369712.1:p.Tyr805His
NM_001382784.1:c.2620T>C	NP_001369713.1:p.Tyr874His
NM_001382785.1:c.2605T>C	NP_001369714.1:p.Tyr869His
NM_001382786.1:c.2584T>C	NP_001369715.1:p.Tyr862His
NM_001382787.1:c.2578T>C	NP_001369716.1:p.Tyr860His
NM_001382788.1:c.2533T>C	NP_001369717.1:p.Tyr845His
NM_001382789.1:c.2524T>C	NP_001369718.1:p.Tyr842His
NM_001382790.1:c.2500T>C	NP_001369719.1:p.Tyr834His
NM_001382791.1:c.2494T>C	NP_001369720.1:p.Tyr832His
NM_001382792.1:c.2467T>C	NP_001369721.1:p.Tyr823His
NM_001382793.1:c.2461T>C	NP_001369722.1:p.Tyr821His
NM_001382794.1:c.2461T>C	NP_001369723.1:p.Tyr821His
NM_001382795.1:c.2455T>C	NP_001369724.1:p.Tyr819His
NM_001382796.1:c.2503T>C	NP_001369725.1:p.Tyr835His
NM_001382797.1:c.2404T>C	NP_001369726.1:p.Tyr802His
NM_001382798.1:c.2493+147T>C	NP_001369727.1:n.2493+147T>C
NM_001382799.1:c.2323T>C	NP_001369728.1:p.Tyr775His
NM_001382800.1:c.2317T>C	NP_001369729.1:p.Tyr773His
NM_001382801.1:c.2445+147T>C	NP_001369730.1:n.2445+147T>C
NM_001382802.1:c.2245T>C	NP_001369731.1:p.Tyr749His
NM_001382803.1:c.2461T>C	NP_001369732.1:p.Tyr821His
NM_001382804.1:c.1675T>C	NP_001369733.1:p.Tyr559His
NM_001382805.1:c.2208+1398T>C	NP_001369734.1:n.2208+1398T>C
NM_001382806.1:c.1465T>C	NP_001369735.1:p.Tyr489His
NM_004448.4:c.2503T>C MANE Select	NP_004439.2:p.Tyr835His
NR_110535.2:n.2741T>C