Canonical Allele Identifier: CA499890085

Gene: ERBB2

Linked Data

• dbSNP Id: rs2145862829
• MyVariant Identifiers: chr17:g.37881322T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39725069T>C , CM000679.2:g.39725069T>C	GRCh38
NC_000017.10:g.37881322T>C , CM000679.1:g.37881322T>C	GRCh37
NC_000017.9:g.35134848T>C	NCBI36
NG_007503.1:g.41930T>C , LRG_724:g.41930T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.2514T>C MANE Select	ENSP00000269571.4:p.Asp838=
ENST00000269571.9:c.2514T>C	ENSP00000269571.4:p.Asp838=
ENST00000406381.6:c.2424T>C	ENSP00000385185.2:p.Asp808=
ENST00000445658.6:c.1686T>C	ENSP00000404047.2:p.Asp562=
ENST00000541774.5:c.2469T>C	ENSP00000446466.1:p.Asp823=
ENST00000578373.5:c.*2304T>C	ENSP00000463427.1:n.*2304T>C
ENST00000580074.1:c.620T>C
ENST00000583038.5:n.3648T>C
ENST00000584450.5:c.2514T>C	ENSP00000463714.1:p.Asp838=
ENST00000584601.5:c.2424T>C	ENSP00000462438.1:p.Asp808=
NM_001005862.2:c.2424T>C , LRG_724t1:c.2424T>C	NP_001005862.1:p.Asp808=
NM_001289936.1:c.2469T>C , LRG_724t4:c.2469T>C	NP_001276865.1:p.Asp823=
NM_001289937.1:c.2514T>C	NP_001276866.1:p.Asp838=
NM_004448.3:c.2514T>C , LRG_724t2:c.2514T>C	NP_004439.2:p.Asp838=
NR_110535.1:n.2838T>C
XM_024450641.1:c.2652T>C	XP_024306409.1:p.Asp884=
XM_024450642.1:c.2607T>C	XP_024306410.1:p.Asp869=
XM_024450643.1:c.2562T>C	XP_024306411.1:p.Asp854=
NM_001005862.3:c.2424T>C	NP_001005862.1:p.Asp808=
NM_001289936.2:c.2469T>C	NP_001276865.1:p.Asp823=
NM_001289937.2:c.2514T>C	NP_001276866.1:p.Asp838=
NM_001382782.1:c.2424T>C	NP_001369711.1:p.Asp808=
NM_001382783.1:c.2424T>C	NP_001369712.1:p.Asp808=
NM_001382784.1:c.2631T>C	NP_001369713.1:p.Asp877=
NM_001382785.1:c.2616T>C	NP_001369714.1:p.Asp872=
NM_001382786.1:c.2595T>C	NP_001369715.1:p.Asp865=
NM_001382787.1:c.2589T>C	NP_001369716.1:p.Asp863=
NM_001382788.1:c.2544T>C	NP_001369717.1:p.Asp848=
NM_001382789.1:c.2535T>C	NP_001369718.1:p.Asp845=
NM_001382790.1:c.2511T>C	NP_001369719.1:p.Asp837=
NM_001382791.1:c.2505T>C	NP_001369720.1:p.Asp835=
NM_001382792.1:c.2478T>C	NP_001369721.1:p.Asp826=
NM_001382793.1:c.2472T>C	NP_001369722.1:p.Asp824=
NM_001382794.1:c.2472T>C	NP_001369723.1:p.Asp824=
NM_001382795.1:c.2466T>C	NP_001369724.1:p.Asp822=
NM_001382796.1:c.2514T>C	NP_001369725.1:p.Asp838=
NM_001382797.1:c.2415T>C	NP_001369726.1:p.Asp805=
NM_001382798.1:c.2493+158T>C	NP_001369727.1:n.2493+158T>C
NM_001382799.1:c.2334T>C	NP_001369728.1:p.Asp778=
NM_001382800.1:c.2328T>C	NP_001369729.1:p.Asp776=
NM_001382801.1:c.2445+158T>C	NP_001369730.1:n.2445+158T>C
NM_001382802.1:c.2256T>C	NP_001369731.1:p.Asp752=
NM_001382803.1:c.2472T>C	NP_001369732.1:p.Asp824=
NM_001382804.1:c.1686T>C	NP_001369733.1:p.Asp562=
NM_001382805.1:c.2208+1409T>C	NP_001369734.1:n.2208+1409T>C
NM_001382806.1:c.1476T>C	NP_001369735.1:p.Asp492=
NM_004448.4:c.2514T>C MANE Select	NP_004439.2:p.Asp838=
NR_110535.2:n.2752T>C