Canonical Allele Identifier: CA399303170

Gene: ERBB2

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.2383C>A MANE Select	ENSP00000269571.4:p.Gln795Lys
ENST00000269571.9:c.2383C>A	ENSP00000269571.4:p.Gln795Lys
ENST00000406381.6:c.2293C>A	ENSP00000385185.2:p.Gln765Lys
ENST00000445658.6:c.1555C>A	ENSP00000404047.2:p.Gln519Lys
ENST00000541774.5:c.2338C>A	ENSP00000446466.1:p.Gln780Lys
ENST00000578373.5:c.*2173C>A	ENSP00000463427.1:n.*2173C>A
ENST00000580074.1:c.489C>A
ENST00000583038.5:n.3517C>A
ENST00000584450.5:c.2383C>A	ENSP00000463714.1:p.Gln795Lys
ENST00000584601.5:c.2293C>A	ENSP00000462438.1:p.Gln765Lys
NM_001005862.2:c.2293C>A , LRG_724t1:c.2293C>A	NP_001005862.1:p.Gln765Lys
NM_001289936.1:c.2338C>A , LRG_724t4:c.2338C>A	NP_001276865.1:p.Gln780Lys
NM_001289937.1:c.2383C>A	NP_001276866.1:p.Gln795Lys
NM_004448.3:c.2383C>A , LRG_724t2:c.2383C>A	NP_004439.2:p.Gln795Lys
NR_110535.1:n.2707C>A
XM_024450641.1:c.2521C>A	XP_024306409.1:p.Gln841Lys
XM_024450642.1:c.2476C>A	XP_024306410.1:p.Gln826Lys
XM_024450643.1:c.2431C>A	XP_024306411.1:p.Gln811Lys
NM_001005862.3:c.2293C>A	NP_001005862.1:p.Gln765Lys
NM_001289936.2:c.2338C>A	NP_001276865.1:p.Gln780Lys
NM_001289937.2:c.2383C>A	NP_001276866.1:p.Gln795Lys
NM_001382782.1:c.2293C>A	NP_001369711.1:p.Gln765Lys
NM_001382783.1:c.2293C>A	NP_001369712.1:p.Gln765Lys
NM_001382784.1:c.2500C>A	NP_001369713.1:p.Gln834Lys
NM_001382785.1:c.2485C>A	NP_001369714.1:p.Gln829Lys
NM_001382786.1:c.2464C>A	NP_001369715.1:p.Gln822Lys
NM_001382787.1:c.2458C>A	NP_001369716.1:p.Gln820Lys
NM_001382788.1:c.2413C>A	NP_001369717.1:p.Gln805Lys
NM_001382789.1:c.2404C>A	NP_001369718.1:p.Gln802Lys
NM_001382790.1:c.2380C>A	NP_001369719.1:p.Gln794Lys
NM_001382791.1:c.2374C>A	NP_001369720.1:p.Gln792Lys
NM_001382792.1:c.2347C>A	NP_001369721.1:p.Gln783Lys
NM_001382793.1:c.2341C>A	NP_001369722.1:p.Gln781Lys
NM_001382794.1:c.2341C>A	NP_001369723.1:p.Gln781Lys
NM_001382795.1:c.2335C>A	NP_001369724.1:p.Gln779Lys
NM_001382796.1:c.2383C>A	NP_001369725.1:p.Gln795Lys
NM_001382797.1:c.2284C>A	NP_001369726.1:p.Gln762Lys
NM_001382798.1:c.2383C>A	NP_001369727.1:p.Gln795Lys
NM_001382799.1:c.2203C>A	NP_001369728.1:p.Gln735Lys
NM_001382800.1:c.2308-248C>A	NP_001369729.1:n.2308-248C>A
NM_001382801.1:c.2335C>A	NP_001369730.1:p.Gln779Lys
NM_001382802.1:c.2125C>A	NP_001369731.1:p.Gln709Lys
NM_001382803.1:c.2341C>A	NP_001369732.1:p.Gln781Lys
NM_001382804.1:c.1555C>A	NP_001369733.1:p.Gln519Lys
NM_001382805.1:c.2208+1141C>A	NP_001369734.1:n.2208+1141C>A
NM_001382806.1:c.1345C>A	NP_001369735.1:p.Gln449Lys
NM_004448.4:c.2383C>A MANE Select	NP_004439.2:p.Gln795Lys
NR_110535.2:n.2621C>A