Canonical Allele Identifier: CA399304241

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37881324T>G (hg19) ; chr17:g.39725071T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39725071T>G , CM000679.2:g.39725071T>G	GRCh38
NC_000017.10:g.37881324T>G , CM000679.1:g.37881324T>G	GRCh37
NC_000017.9:g.35134850T>G	NCBI36
NG_007503.1:g.41932T>G , LRG_724:g.41932T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.2516T>G MANE Select	ENSP00000269571.4:p.Val839Gly
ENST00000269571.9:c.2516T>G	ENSP00000269571.4:p.Val839Gly
ENST00000406381.6:c.2426T>G	ENSP00000385185.2:p.Val809Gly
ENST00000445658.6:c.1688T>G	ENSP00000404047.2:p.Val563Gly
ENST00000541774.5:c.2471T>G	ENSP00000446466.1:p.Val824Gly
ENST00000578373.5:c.*2306T>G	ENSP00000463427.1:n.*2306T>G
ENST00000580074.1:c.622T>G
ENST00000583038.5:n.3650T>G
ENST00000584450.5:c.2516T>G	ENSP00000463714.1:p.Val839Gly
ENST00000584601.5:c.2426T>G	ENSP00000462438.1:p.Val809Gly
NM_001005862.2:c.2426T>G , LRG_724t1:c.2426T>G	NP_001005862.1:p.Val809Gly
NM_001289936.1:c.2471T>G , LRG_724t4:c.2471T>G	NP_001276865.1:p.Val824Gly
NM_001289937.1:c.2516T>G	NP_001276866.1:p.Val839Gly
NM_004448.3:c.2516T>G , LRG_724t2:c.2516T>G	NP_004439.2:p.Val839Gly
NR_110535.1:n.2840T>G
XM_024450641.1:c.2654T>G	XP_024306409.1:p.Val885Gly
XM_024450642.1:c.2609T>G	XP_024306410.1:p.Val870Gly
XM_024450643.1:c.2564T>G	XP_024306411.1:p.Val855Gly
NM_001005862.3:c.2426T>G	NP_001005862.1:p.Val809Gly
NM_001289936.2:c.2471T>G	NP_001276865.1:p.Val824Gly
NM_001289937.2:c.2516T>G	NP_001276866.1:p.Val839Gly
NM_001382782.1:c.2426T>G	NP_001369711.1:p.Val809Gly
NM_001382783.1:c.2426T>G	NP_001369712.1:p.Val809Gly
NM_001382784.1:c.2633T>G	NP_001369713.1:p.Val878Gly
NM_001382785.1:c.2618T>G	NP_001369714.1:p.Val873Gly
NM_001382786.1:c.2597T>G	NP_001369715.1:p.Val866Gly
NM_001382787.1:c.2591T>G	NP_001369716.1:p.Val864Gly
NM_001382788.1:c.2546T>G	NP_001369717.1:p.Val849Gly
NM_001382789.1:c.2537T>G	NP_001369718.1:p.Val846Gly
NM_001382790.1:c.2513T>G	NP_001369719.1:p.Val838Gly
NM_001382791.1:c.2507T>G	NP_001369720.1:p.Val836Gly
NM_001382792.1:c.2480T>G	NP_001369721.1:p.Val827Gly
NM_001382793.1:c.2474T>G	NP_001369722.1:p.Val825Gly
NM_001382794.1:c.2474T>G	NP_001369723.1:p.Val825Gly
NM_001382795.1:c.2468T>G	NP_001369724.1:p.Val823Gly
NM_001382796.1:c.2516T>G	NP_001369725.1:p.Val839Gly
NM_001382797.1:c.2417T>G	NP_001369726.1:p.Val806Gly
NM_001382798.1:c.2493+160T>G	NP_001369727.1:n.2493+160T>G
NM_001382799.1:c.2336T>G	NP_001369728.1:p.Val779Gly
NM_001382800.1:c.2330T>G	NP_001369729.1:p.Val777Gly
NM_001382801.1:c.2445+160T>G	NP_001369730.1:n.2445+160T>G
NM_001382802.1:c.2258T>G	NP_001369731.1:p.Val753Gly
NM_001382803.1:c.2474T>G	NP_001369732.1:p.Val825Gly
NM_001382804.1:c.1688T>G	NP_001369733.1:p.Val563Gly
NM_001382805.1:c.2208+1411T>G	NP_001369734.1:n.2208+1411T>G
NM_001382806.1:c.1478T>G	NP_001369735.1:p.Val493Gly
NM_004448.4:c.2516T>G MANE Select	NP_004439.2:p.Val839Gly
NR_110535.2:n.2754T>G