Canonical Allele Identifier: CA399304371

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37881342A>G (hg19) ; chr17:g.39725089A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39725089A>G , CM000679.2:g.39725089A>G	GRCh38
NC_000017.10:g.37881342A>G , CM000679.1:g.37881342A>G	GRCh37
NC_000017.9:g.35134868A>G	NCBI36
NG_007503.1:g.41950A>G , LRG_724:g.41950A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.2534A>G MANE Select	ENSP00000269571.4:p.Asp845Gly
ENST00000269571.9:c.2534A>G	ENSP00000269571.4:p.Asp845Gly
ENST00000406381.6:c.2444A>G	ENSP00000385185.2:p.Asp815Gly
ENST00000445658.6:c.1706A>G	ENSP00000404047.2:p.Asp569Gly
ENST00000541774.5:c.2489A>G	ENSP00000446466.1:p.Asp830Gly
ENST00000578373.5:c.*2324A>G	ENSP00000463427.1:n.*2324A>G
ENST00000580074.1:c.640A>G
ENST00000583038.5:n.3668A>G
ENST00000584450.5:c.2534A>G	ENSP00000463714.1:p.Asp845Gly
ENST00000584601.5:c.2444A>G	ENSP00000462438.1:p.Asp815Gly
NM_001005862.2:c.2444A>G , LRG_724t1:c.2444A>G	NP_001005862.1:p.Asp815Gly
NM_001289936.1:c.2489A>G , LRG_724t4:c.2489A>G	NP_001276865.1:p.Asp830Gly
NM_001289937.1:c.2534A>G	NP_001276866.1:p.Asp845Gly
NM_004448.3:c.2534A>G , LRG_724t2:c.2534A>G	NP_004439.2:p.Asp845Gly
NR_110535.1:n.2858A>G
XM_024450641.1:c.2672A>G	XP_024306409.1:p.Asp891Gly
XM_024450642.1:c.2627A>G	XP_024306410.1:p.Asp876Gly
XM_024450643.1:c.2582A>G	XP_024306411.1:p.Asp861Gly
NM_001005862.3:c.2444A>G	NP_001005862.1:p.Asp815Gly
NM_001289936.2:c.2489A>G	NP_001276865.1:p.Asp830Gly
NM_001289937.2:c.2534A>G	NP_001276866.1:p.Asp845Gly
NM_001382782.1:c.2444A>G	NP_001369711.1:p.Asp815Gly
NM_001382783.1:c.2444A>G	NP_001369712.1:p.Asp815Gly
NM_001382784.1:c.2651A>G	NP_001369713.1:p.Asp884Gly
NM_001382785.1:c.2636A>G	NP_001369714.1:p.Asp879Gly
NM_001382786.1:c.2615A>G	NP_001369715.1:p.Asp872Gly
NM_001382787.1:c.2609A>G	NP_001369716.1:p.Asp870Gly
NM_001382788.1:c.2564A>G	NP_001369717.1:p.Asp855Gly
NM_001382789.1:c.2555A>G	NP_001369718.1:p.Asp852Gly
NM_001382790.1:c.2531A>G	NP_001369719.1:p.Asp844Gly
NM_001382791.1:c.2525A>G	NP_001369720.1:p.Asp842Gly
NM_001382792.1:c.2498A>G	NP_001369721.1:p.Asp833Gly
NM_001382793.1:c.2492A>G	NP_001369722.1:p.Asp831Gly
NM_001382794.1:c.2492A>G	NP_001369723.1:p.Asp831Gly
NM_001382795.1:c.2486A>G	NP_001369724.1:p.Asp829Gly
NM_001382796.1:c.2534A>G	NP_001369725.1:p.Asp845Gly
NM_001382797.1:c.2435A>G	NP_001369726.1:p.Asp812Gly
NM_001382798.1:c.2493+178A>G	NP_001369727.1:n.2493+178A>G
NM_001382799.1:c.2354A>G	NP_001369728.1:p.Asp785Gly
NM_001382800.1:c.2348A>G	NP_001369729.1:p.Asp783Gly
NM_001382801.1:c.2445+178A>G	NP_001369730.1:n.2445+178A>G
NM_001382802.1:c.2276A>G	NP_001369731.1:p.Asp759Gly
NM_001382803.1:c.2492A>G	NP_001369732.1:p.Asp831Gly
NM_001382804.1:c.1706A>G	NP_001369733.1:p.Asp569Gly
NM_001382805.1:c.2208+1429A>G	NP_001369734.1:n.2208+1429A>G
NM_001382806.1:c.1496A>G	NP_001369735.1:p.Asp499Gly
NM_004448.4:c.2534A>G MANE Select	NP_004439.2:p.Asp845Gly
NR_110535.2:n.2772A>G