Canonical Allele Identifier: CA499670910

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37881089C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39724836C>T , CM000679.2:g.39724836C>T	GRCh38
NC_000017.10:g.37881089C>T , CM000679.1:g.37881089C>T	GRCh37
NC_000017.9:g.35134615C>T	NCBI36
NG_007503.1:g.41697C>T , LRG_724:g.41697C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.2418C>T MANE Select	ENSP00000269571.4:p.Leu806=
ENST00000269571.9:c.2418C>T	ENSP00000269571.4:p.Leu806=
ENST00000406381.6:c.2328C>T	ENSP00000385185.2:p.Leu776=
ENST00000445658.6:c.1590C>T	ENSP00000404047.2:p.Leu530=
ENST00000541774.5:c.2373C>T	ENSP00000446466.1:p.Leu791=
ENST00000578373.5:c.*2208C>T	ENSP00000463427.1:n.*2208C>T
ENST00000580074.1:c.524C>T
ENST00000583038.5:n.3552C>T
ENST00000584450.5:c.2418C>T	ENSP00000463714.1:p.Leu806=
ENST00000584601.5:c.2328C>T	ENSP00000462438.1:p.Leu776=
NM_001005862.2:c.2328C>T , LRG_724t1:c.2328C>T	NP_001005862.1:p.Leu776=
NM_001289936.1:c.2373C>T , LRG_724t4:c.2373C>T	NP_001276865.1:p.Leu791=
NM_001289937.1:c.2418C>T	NP_001276866.1:p.Leu806=
NM_004448.3:c.2418C>T , LRG_724t2:c.2418C>T	NP_004439.2:p.Leu806=
NR_110535.1:n.2742C>T
XM_024450641.1:c.2556C>T	XP_024306409.1:p.Leu852=
XM_024450642.1:c.2511C>T	XP_024306410.1:p.Leu837=
XM_024450643.1:c.2466C>T	XP_024306411.1:p.Leu822=
NM_001005862.3:c.2328C>T	NP_001005862.1:p.Leu776=
NM_001289936.2:c.2373C>T	NP_001276865.1:p.Leu791=
NM_001289937.2:c.2418C>T	NP_001276866.1:p.Leu806=
NM_001382782.1:c.2328C>T	NP_001369711.1:p.Leu776=
NM_001382783.1:c.2328C>T	NP_001369712.1:p.Leu776=
NM_001382784.1:c.2535C>T	NP_001369713.1:p.Leu845=
NM_001382785.1:c.2520C>T	NP_001369714.1:p.Leu840=
NM_001382786.1:c.2499C>T	NP_001369715.1:p.Leu833=
NM_001382787.1:c.2493C>T	NP_001369716.1:p.Leu831=
NM_001382788.1:c.2448C>T	NP_001369717.1:p.Leu816=
NM_001382789.1:c.2439C>T	NP_001369718.1:p.Leu813=
NM_001382790.1:c.2415C>T	NP_001369719.1:p.Leu805=
NM_001382791.1:c.2409C>T	NP_001369720.1:p.Leu803=
NM_001382792.1:c.2382C>T	NP_001369721.1:p.Leu794=
NM_001382793.1:c.2376C>T	NP_001369722.1:p.Leu792=
NM_001382794.1:c.2376C>T	NP_001369723.1:p.Leu792=
NM_001382795.1:c.2370C>T	NP_001369724.1:p.Leu790=
NM_001382796.1:c.2418C>T	NP_001369725.1:p.Leu806=
NM_001382797.1:c.2319C>T	NP_001369726.1:p.Leu773=
NM_001382798.1:c.2418C>T	NP_001369727.1:p.Leu806=
NM_001382799.1:c.2238C>T	NP_001369728.1:p.Leu746=
NM_001382800.1:c.2308-213C>T	NP_001369729.1:n.2308-213C>T
NM_001382801.1:c.2370C>T	NP_001369730.1:p.Leu790=
NM_001382802.1:c.2160C>T	NP_001369731.1:p.Leu720=
NM_001382803.1:c.2376C>T	NP_001369732.1:p.Leu792=
NM_001382804.1:c.1590C>T	NP_001369733.1:p.Leu530=
NM_001382805.1:c.2208+1176C>T	NP_001369734.1:n.2208+1176C>T
NM_001382806.1:c.1380C>T	NP_001369735.1:p.Leu460=
NM_004448.4:c.2418C>T MANE Select	NP_004439.2:p.Leu806=
NR_110535.2:n.2656C>T