Canonical Allele Identifier: CA399303370

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37881086C>A (hg19) ; chr17:g.39724833C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39724833C>A , CM000679.2:g.39724833C>A	GRCh38
NC_000017.10:g.37881086C>A , CM000679.1:g.37881086C>A	GRCh37
NC_000017.9:g.35134612C>A	NCBI36
NG_007503.1:g.41694C>A , LRG_724:g.41694C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.2415C>A MANE Select	ENSP00000269571.4:p.Cys805Ter
ENST00000269571.9:c.2415C>A	ENSP00000269571.4:p.Cys805Ter
ENST00000406381.6:c.2325C>A	ENSP00000385185.2:p.Cys775Ter
ENST00000445658.6:c.1587C>A	ENSP00000404047.2:p.Cys529Ter
ENST00000541774.5:c.2370C>A	ENSP00000446466.1:p.Cys790Ter
ENST00000578373.5:c.*2205C>A	ENSP00000463427.1:n.*2205C>A
ENST00000580074.1:c.521C>A
ENST00000583038.5:n.3549C>A
ENST00000584450.5:c.2415C>A	ENSP00000463714.1:p.Cys805Ter
ENST00000584601.5:c.2325C>A	ENSP00000462438.1:p.Cys775Ter
NM_001005862.2:c.2325C>A , LRG_724t1:c.2325C>A	NP_001005862.1:p.Cys775Ter
NM_001289936.1:c.2370C>A , LRG_724t4:c.2370C>A	NP_001276865.1:p.Cys790Ter
NM_001289937.1:c.2415C>A	NP_001276866.1:p.Cys805Ter
NM_004448.3:c.2415C>A , LRG_724t2:c.2415C>A	NP_004439.2:p.Cys805Ter
NR_110535.1:n.2739C>A
XM_024450641.1:c.2553C>A	XP_024306409.1:p.Cys851Ter
XM_024450642.1:c.2508C>A	XP_024306410.1:p.Cys836Ter
XM_024450643.1:c.2463C>A	XP_024306411.1:p.Cys821Ter
NM_001005862.3:c.2325C>A	NP_001005862.1:p.Cys775Ter
NM_001289936.2:c.2370C>A	NP_001276865.1:p.Cys790Ter
NM_001289937.2:c.2415C>A	NP_001276866.1:p.Cys805Ter
NM_001382782.1:c.2325C>A	NP_001369711.1:p.Cys775Ter
NM_001382783.1:c.2325C>A	NP_001369712.1:p.Cys775Ter
NM_001382784.1:c.2532C>A	NP_001369713.1:p.Cys844Ter
NM_001382785.1:c.2517C>A	NP_001369714.1:p.Cys839Ter
NM_001382786.1:c.2496C>A	NP_001369715.1:p.Cys832Ter
NM_001382787.1:c.2490C>A	NP_001369716.1:p.Cys830Ter
NM_001382788.1:c.2445C>A	NP_001369717.1:p.Cys815Ter
NM_001382789.1:c.2436C>A	NP_001369718.1:p.Cys812Ter
NM_001382790.1:c.2412C>A	NP_001369719.1:p.Cys804Ter
NM_001382791.1:c.2406C>A	NP_001369720.1:p.Cys802Ter
NM_001382792.1:c.2379C>A	NP_001369721.1:p.Cys793Ter
NM_001382793.1:c.2373C>A	NP_001369722.1:p.Cys791Ter
NM_001382794.1:c.2373C>A	NP_001369723.1:p.Cys791Ter
NM_001382795.1:c.2367C>A	NP_001369724.1:p.Cys789Ter
NM_001382796.1:c.2415C>A	NP_001369725.1:p.Cys805Ter
NM_001382797.1:c.2316C>A	NP_001369726.1:p.Cys772Ter
NM_001382798.1:c.2415C>A	NP_001369727.1:p.Cys805Ter
NM_001382799.1:c.2235C>A	NP_001369728.1:p.Cys745Ter
NM_001382800.1:c.2308-216C>A	NP_001369729.1:n.2308-216C>A
NM_001382801.1:c.2367C>A	NP_001369730.1:p.Cys789Ter
NM_001382802.1:c.2157C>A	NP_001369731.1:p.Cys719Ter
NM_001382803.1:c.2373C>A	NP_001369732.1:p.Cys791Ter
NM_001382804.1:c.1587C>A	NP_001369733.1:p.Cys529Ter
NM_001382805.1:c.2208+1173C>A	NP_001369734.1:n.2208+1173C>A
NM_001382806.1:c.1377C>A	NP_001369735.1:p.Cys459Ter
NM_004448.4:c.2415C>A MANE Select	NP_004439.2:p.Cys805Ter
NR_110535.2:n.2653C>A