Canonical Allele Identifier: CA399302906

Gene: ERBB2

Linked Data

• dbSNP Id: rs2145848497
• MyVariant Identifiers: chr17:g.37881014T>G (hg19) ; chr17:g.39724761T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39724761T>G , CM000679.2:g.39724761T>G	GRCh38
NC_000017.10:g.37881014T>G , CM000679.1:g.37881014T>G	GRCh37
NC_000017.9:g.35134540T>G	NCBI36
NG_007503.1:g.41622T>G , LRG_724:g.41622T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.2343T>G MANE Select	ENSP00000269571.4:p.Tyr781Ter
ENST00000269571.9:c.2343T>G	ENSP00000269571.4:p.Tyr781Ter
ENST00000406381.6:c.2253T>G	ENSP00000385185.2:p.Tyr751Ter
ENST00000445658.6:c.1515T>G	ENSP00000404047.2:p.Tyr505Ter
ENST00000541774.5:c.2298T>G	ENSP00000446466.1:p.Tyr766Ter
ENST00000578373.5:c.*2133T>G	ENSP00000463427.1:n.*2133T>G
ENST00000580074.1:c.449T>G
ENST00000583038.5:n.3477T>G
ENST00000584450.5:c.2343T>G	ENSP00000463714.1:p.Tyr781Ter
ENST00000584601.5:c.2253T>G	ENSP00000462438.1:p.Tyr751Ter
NM_001005862.2:c.2253T>G , LRG_724t1:c.2253T>G	NP_001005862.1:p.Tyr751Ter
NM_001289936.1:c.2298T>G , LRG_724t4:c.2298T>G	NP_001276865.1:p.Tyr766Ter
NM_001289937.1:c.2343T>G	NP_001276866.1:p.Tyr781Ter
NM_004448.3:c.2343T>G , LRG_724t2:c.2343T>G	NP_004439.2:p.Tyr781Ter
NR_110535.1:n.2667T>G
XM_024450641.1:c.2481T>G	XP_024306409.1:p.Tyr827Ter
XM_024450642.1:c.2436T>G	XP_024306410.1:p.Tyr812Ter
XM_024450643.1:c.2391T>G	XP_024306411.1:p.Tyr797Ter
NM_001005862.3:c.2253T>G	NP_001005862.1:p.Tyr751Ter
NM_001289936.2:c.2298T>G	NP_001276865.1:p.Tyr766Ter
NM_001289937.2:c.2343T>G	NP_001276866.1:p.Tyr781Ter
NM_001382782.1:c.2253T>G	NP_001369711.1:p.Tyr751Ter
NM_001382783.1:c.2253T>G	NP_001369712.1:p.Tyr751Ter
NM_001382784.1:c.2460T>G	NP_001369713.1:p.Tyr820Ter
NM_001382785.1:c.2445T>G	NP_001369714.1:p.Tyr815Ter
NM_001382786.1:c.2424T>G	NP_001369715.1:p.Tyr808Ter
NM_001382787.1:c.2418T>G	NP_001369716.1:p.Tyr806Ter
NM_001382788.1:c.2373T>G	NP_001369717.1:p.Tyr791Ter
NM_001382789.1:c.2364T>G	NP_001369718.1:p.Tyr788Ter
NM_001382790.1:c.2340T>G	NP_001369719.1:p.Tyr780Ter
NM_001382791.1:c.2334T>G	NP_001369720.1:p.Tyr778Ter
NM_001382792.1:c.2307T>G	NP_001369721.1:p.Tyr769Ter
NM_001382793.1:c.2301T>G	NP_001369722.1:p.Tyr767Ter
NM_001382794.1:c.2301T>G	NP_001369723.1:p.Tyr767Ter
NM_001382795.1:c.2295T>G	NP_001369724.1:p.Tyr765Ter
NM_001382796.1:c.2343T>G	NP_001369725.1:p.Tyr781Ter
NM_001382797.1:c.2244T>G	NP_001369726.1:p.Tyr748Ter
NM_001382798.1:c.2343T>G	NP_001369727.1:p.Tyr781Ter
NM_001382799.1:c.2163T>G	NP_001369728.1:p.Tyr721Ter
NM_001382800.1:c.2308-288T>G	NP_001369729.1:n.2308-288T>G
NM_001382801.1:c.2295T>G	NP_001369730.1:p.Tyr765Ter
NM_001382802.1:c.2085T>G	NP_001369731.1:p.Tyr695Ter
NM_001382803.1:c.2301T>G	NP_001369732.1:p.Tyr767Ter
NM_001382804.1:c.1515T>G	NP_001369733.1:p.Tyr505Ter
NM_001382805.1:c.2208+1101T>G	NP_001369734.1:n.2208+1101T>G
NM_001382806.1:c.1305T>G	NP_001369735.1:p.Tyr435Ter
NM_004448.4:c.2343T>G MANE Select	NP_004439.2:p.Tyr781Ter
NR_110535.2:n.2581T>G