Canonical Allele Identifier: CA399304067

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37881302G>T (hg19) ; chr17:g.39725049G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39725049G>T , CM000679.2:g.39725049G>T	GRCh38
NC_000017.10:g.37881302G>T , CM000679.1:g.37881302G>T	GRCh37
NC_000017.9:g.35134828G>T	NCBI36
NG_007503.1:g.41910G>T , LRG_724:g.41910G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000269571.10:c.2494G>T MANE Select	ENSP00000269571.4:p.Gly832Trp
ENST00000269571.9:c.2494G>T	ENSP00000269571.4:p.Gly832Trp
ENST00000406381.6:c.2404G>T	ENSP00000385185.2:p.Gly802Trp
ENST00000445658.6:c.1666G>T	ENSP00000404047.2:p.Gly556Trp
ENST00000541774.5:c.2449G>T	ENSP00000446466.1:p.Gly817Trp
ENST00000578373.5:c.*2284G>T	ENSP00000463427.1:n.*2284G>T
ENST00000580074.1:c.600G>T
ENST00000583038.5:n.3628G>T
ENST00000584450.5:c.2494G>T	ENSP00000463714.1:p.Gly832Trp
ENST00000584601.5:c.2404G>T	ENSP00000462438.1:p.Gly802Trp
NM_001005862.2:c.2404G>T , LRG_724t1:c.2404G>T	NP_001005862.1:p.Gly802Trp
NM_001289936.1:c.2449G>T , LRG_724t4:c.2449G>T	NP_001276865.1:p.Gly817Trp
NM_001289937.1:c.2494G>T	NP_001276866.1:p.Gly832Trp
NM_004448.3:c.2494G>T , LRG_724t2:c.2494G>T	NP_004439.2:p.Gly832Trp
NR_110535.1:n.2818G>T
XM_024450641.1:c.2632G>T	XP_024306409.1:p.Gly878Trp
XM_024450642.1:c.2587G>T	XP_024306410.1:p.Gly863Trp
XM_024450643.1:c.2542G>T	XP_024306411.1:p.Gly848Trp
NM_001005862.3:c.2404G>T	NP_001005862.1:p.Gly802Trp
NM_001289936.2:c.2449G>T	NP_001276865.1:p.Gly817Trp
NM_001289937.2:c.2494G>T	NP_001276866.1:p.Gly832Trp
NM_001382782.1:c.2404G>T	NP_001369711.1:p.Gly802Trp
NM_001382783.1:c.2404G>T	NP_001369712.1:p.Gly802Trp
NM_001382784.1:c.2611G>T	NP_001369713.1:p.Gly871Trp
NM_001382785.1:c.2596G>T	NP_001369714.1:p.Gly866Trp
NM_001382786.1:c.2575G>T	NP_001369715.1:p.Gly859Trp
NM_001382787.1:c.2569G>T	NP_001369716.1:p.Gly857Trp
NM_001382788.1:c.2524G>T	NP_001369717.1:p.Gly842Trp
NM_001382789.1:c.2515G>T	NP_001369718.1:p.Gly839Trp
NM_001382790.1:c.2491G>T	NP_001369719.1:p.Gly831Trp
NM_001382791.1:c.2485G>T	NP_001369720.1:p.Gly829Trp
NM_001382792.1:c.2458G>T	NP_001369721.1:p.Gly820Trp
NM_001382793.1:c.2452G>T	NP_001369722.1:p.Gly818Trp
NM_001382794.1:c.2452G>T	NP_001369723.1:p.Gly818Trp
NM_001382795.1:c.2446G>T	NP_001369724.1:p.Gly816Trp
NM_001382796.1:c.2494G>T	NP_001369725.1:p.Gly832Trp
NM_001382797.1:c.2395G>T	NP_001369726.1:p.Gly799Trp
NM_001382798.1:c.2493+138G>T	NP_001369727.1:n.2493+138G>T
NM_001382799.1:c.2314G>T	NP_001369728.1:p.Gly772Trp
NM_001382800.1:c.2308G>T	NP_001369729.1:p.Gly770Trp
NM_001382801.1:c.2445+138G>T	NP_001369730.1:n.2445+138G>T
NM_001382802.1:c.2236G>T	NP_001369731.1:p.Gly746Trp
NM_001382803.1:c.2452G>T	NP_001369732.1:p.Gly818Trp
NM_001382804.1:c.1666G>T	NP_001369733.1:p.Gly556Trp
NM_001382805.1:c.2208+1389G>T	NP_001369734.1:n.2208+1389G>T
NM_001382806.1:c.1456G>T	NP_001369735.1:p.Gly486Trp
NM_004448.4:c.2494G>T MANE Select	NP_004439.2:p.Gly832Trp
NR_110535.2:n.2732G>T