Canonical Allele Identifier: CA399303173

Gene: ERBB2

Linked Data

• dbSNP Id: rs924725638
• MyVariant Identifiers: chr17:g.37881054C>G (hg19) ; chr17:g.39724801C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39724801C>G , CM000679.2:g.39724801C>G	GRCh38
NC_000017.10:g.37881054C>G , CM000679.1:g.37881054C>G	GRCh37
NC_000017.9:g.35134580C>G	NCBI36
NG_007503.1:g.41662C>G , LRG_724:g.41662C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.2383C>G MANE Select	ENSP00000269571.4:p.Gln795Glu
ENST00000269571.9:c.2383C>G	ENSP00000269571.4:p.Gln795Glu
ENST00000406381.6:c.2293C>G	ENSP00000385185.2:p.Gln765Glu
ENST00000445658.6:c.1555C>G	ENSP00000404047.2:p.Gln519Glu
ENST00000541774.5:c.2338C>G	ENSP00000446466.1:p.Gln780Glu
ENST00000578373.5:c.*2173C>G	ENSP00000463427.1:n.*2173C>G
ENST00000580074.1:c.489C>G
ENST00000583038.5:n.3517C>G
ENST00000584450.5:c.2383C>G	ENSP00000463714.1:p.Gln795Glu
ENST00000584601.5:c.2293C>G	ENSP00000462438.1:p.Gln765Glu
NM_001005862.2:c.2293C>G , LRG_724t1:c.2293C>G	NP_001005862.1:p.Gln765Glu
NM_001289936.1:c.2338C>G , LRG_724t4:c.2338C>G	NP_001276865.1:p.Gln780Glu
NM_001289937.1:c.2383C>G	NP_001276866.1:p.Gln795Glu
NM_004448.3:c.2383C>G , LRG_724t2:c.2383C>G	NP_004439.2:p.Gln795Glu
NR_110535.1:n.2707C>G
XM_024450641.1:c.2521C>G	XP_024306409.1:p.Gln841Glu
XM_024450642.1:c.2476C>G	XP_024306410.1:p.Gln826Glu
XM_024450643.1:c.2431C>G	XP_024306411.1:p.Gln811Glu
NM_001005862.3:c.2293C>G	NP_001005862.1:p.Gln765Glu
NM_001289936.2:c.2338C>G	NP_001276865.1:p.Gln780Glu
NM_001289937.2:c.2383C>G	NP_001276866.1:p.Gln795Glu
NM_001382782.1:c.2293C>G	NP_001369711.1:p.Gln765Glu
NM_001382783.1:c.2293C>G	NP_001369712.1:p.Gln765Glu
NM_001382784.1:c.2500C>G	NP_001369713.1:p.Gln834Glu
NM_001382785.1:c.2485C>G	NP_001369714.1:p.Gln829Glu
NM_001382786.1:c.2464C>G	NP_001369715.1:p.Gln822Glu
NM_001382787.1:c.2458C>G	NP_001369716.1:p.Gln820Glu
NM_001382788.1:c.2413C>G	NP_001369717.1:p.Gln805Glu
NM_001382789.1:c.2404C>G	NP_001369718.1:p.Gln802Glu
NM_001382790.1:c.2380C>G	NP_001369719.1:p.Gln794Glu
NM_001382791.1:c.2374C>G	NP_001369720.1:p.Gln792Glu
NM_001382792.1:c.2347C>G	NP_001369721.1:p.Gln783Glu
NM_001382793.1:c.2341C>G	NP_001369722.1:p.Gln781Glu
NM_001382794.1:c.2341C>G	NP_001369723.1:p.Gln781Glu
NM_001382795.1:c.2335C>G	NP_001369724.1:p.Gln779Glu
NM_001382796.1:c.2383C>G	NP_001369725.1:p.Gln795Glu
NM_001382797.1:c.2284C>G	NP_001369726.1:p.Gln762Glu
NM_001382798.1:c.2383C>G	NP_001369727.1:p.Gln795Glu
NM_001382799.1:c.2203C>G	NP_001369728.1:p.Gln735Glu
NM_001382800.1:c.2308-248C>G	NP_001369729.1:n.2308-248C>G
NM_001382801.1:c.2335C>G	NP_001369730.1:p.Gln779Glu
NM_001382802.1:c.2125C>G	NP_001369731.1:p.Gln709Glu
NM_001382803.1:c.2341C>G	NP_001369732.1:p.Gln781Glu
NM_001382804.1:c.1555C>G	NP_001369733.1:p.Gln519Glu
NM_001382805.1:c.2208+1141C>G	NP_001369734.1:n.2208+1141C>G
NM_001382806.1:c.1345C>G	NP_001369735.1:p.Gln449Glu
NM_004448.4:c.2383C>G MANE Select	NP_004439.2:p.Gln795Glu
NR_110535.2:n.2621C>G