Canonical Allele Identifier: CA399304293

Gene: ERBB2

Linked Data

• dbSNP Id: rs2145863267
• MyVariant Identifiers: chr17:g.37881333T>G (hg19) ; chr17:g.39725080T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39725080T>G , CM000679.2:g.39725080T>G	GRCh38
NC_000017.10:g.37881333T>G , CM000679.1:g.37881333T>G	GRCh37
NC_000017.9:g.35134859T>G	NCBI36
NG_007503.1:g.41941T>G , LRG_724:g.41941T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.2525T>G MANE Select	ENSP00000269571.4:p.Val842Gly
ENST00000269571.9:c.2525T>G	ENSP00000269571.4:p.Val842Gly
ENST00000406381.6:c.2435T>G	ENSP00000385185.2:p.Val812Gly
ENST00000445658.6:c.1697T>G	ENSP00000404047.2:p.Val566Gly
ENST00000541774.5:c.2480T>G	ENSP00000446466.1:p.Val827Gly
ENST00000578373.5:c.*2315T>G	ENSP00000463427.1:n.*2315T>G
ENST00000580074.1:c.631T>G
ENST00000583038.5:n.3659T>G
ENST00000584450.5:c.2525T>G	ENSP00000463714.1:p.Val842Gly
ENST00000584601.5:c.2435T>G	ENSP00000462438.1:p.Val812Gly
NM_001005862.2:c.2435T>G , LRG_724t1:c.2435T>G	NP_001005862.1:p.Val812Gly
NM_001289936.1:c.2480T>G , LRG_724t4:c.2480T>G	NP_001276865.1:p.Val827Gly
NM_001289937.1:c.2525T>G	NP_001276866.1:p.Val842Gly
NM_004448.3:c.2525T>G , LRG_724t2:c.2525T>G	NP_004439.2:p.Val842Gly
NR_110535.1:n.2849T>G
XM_024450641.1:c.2663T>G	XP_024306409.1:p.Val888Gly
XM_024450642.1:c.2618T>G	XP_024306410.1:p.Val873Gly
XM_024450643.1:c.2573T>G	XP_024306411.1:p.Val858Gly
NM_001005862.3:c.2435T>G	NP_001005862.1:p.Val812Gly
NM_001289936.2:c.2480T>G	NP_001276865.1:p.Val827Gly
NM_001289937.2:c.2525T>G	NP_001276866.1:p.Val842Gly
NM_001382782.1:c.2435T>G	NP_001369711.1:p.Val812Gly
NM_001382783.1:c.2435T>G	NP_001369712.1:p.Val812Gly
NM_001382784.1:c.2642T>G	NP_001369713.1:p.Val881Gly
NM_001382785.1:c.2627T>G	NP_001369714.1:p.Val876Gly
NM_001382786.1:c.2606T>G	NP_001369715.1:p.Val869Gly
NM_001382787.1:c.2600T>G	NP_001369716.1:p.Val867Gly
NM_001382788.1:c.2555T>G	NP_001369717.1:p.Val852Gly
NM_001382789.1:c.2546T>G	NP_001369718.1:p.Val849Gly
NM_001382790.1:c.2522T>G	NP_001369719.1:p.Val841Gly
NM_001382791.1:c.2516T>G	NP_001369720.1:p.Val839Gly
NM_001382792.1:c.2489T>G	NP_001369721.1:p.Val830Gly
NM_001382793.1:c.2483T>G	NP_001369722.1:p.Val828Gly
NM_001382794.1:c.2483T>G	NP_001369723.1:p.Val828Gly
NM_001382795.1:c.2477T>G	NP_001369724.1:p.Val826Gly
NM_001382796.1:c.2525T>G	NP_001369725.1:p.Val842Gly
NM_001382797.1:c.2426T>G	NP_001369726.1:p.Val809Gly
NM_001382798.1:c.2493+169T>G	NP_001369727.1:n.2493+169T>G
NM_001382799.1:c.2345T>G	NP_001369728.1:p.Val782Gly
NM_001382800.1:c.2339T>G	NP_001369729.1:p.Val780Gly
NM_001382801.1:c.2445+169T>G	NP_001369730.1:n.2445+169T>G
NM_001382802.1:c.2267T>G	NP_001369731.1:p.Val756Gly
NM_001382803.1:c.2483T>G	NP_001369732.1:p.Val828Gly
NM_001382804.1:c.1697T>G	NP_001369733.1:p.Val566Gly
NM_001382805.1:c.2208+1420T>G	NP_001369734.1:n.2208+1420T>G
NM_001382806.1:c.1487T>G	NP_001369735.1:p.Val496Gly
NM_004448.4:c.2525T>G MANE Select	NP_004439.2:p.Val842Gly
NR_110535.2:n.2763T>G