Canonical Allele Identifier: CA499890173

Gene: ERBB2

Linked Data

• dbSNP Id: rs2145865615
• MyVariant Identifiers: chr17:g.37881391T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39725138T>C , CM000679.2:g.39725138T>C	GRCh38
NC_000017.10:g.37881391T>C , CM000679.1:g.37881391T>C	GRCh37
NC_000017.9:g.35134917T>C	NCBI36
NG_007503.1:g.41999T>C , LRG_724:g.41999T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000269571.10:c.2583T>C MANE Select	ENSP00000269571.4:p.Ile861=
ENST00000269571.9:c.2583T>C	ENSP00000269571.4:p.Ile861=
ENST00000406381.6:c.2493T>C	ENSP00000385185.2:p.Ile831=
ENST00000445658.6:c.1755T>C	ENSP00000404047.2:p.Ile585=
ENST00000541774.5:c.2538T>C	ENSP00000446466.1:p.Ile846=
ENST00000578373.5:c.*2373T>C	ENSP00000463427.1:n.*2373T>C
ENST00000580074.1:c.689T>C
ENST00000583038.5:n.3717T>C
ENST00000584450.5:c.2583T>C	ENSP00000463714.1:p.Ile861=
ENST00000584601.5:c.2493T>C	ENSP00000462438.1:p.Ile831=
NM_001005862.2:c.2493T>C , LRG_724t1:c.2493T>C	NP_001005862.1:p.Ile831=
NM_001289936.1:c.2538T>C , LRG_724t4:c.2538T>C	NP_001276865.1:p.Ile846=
NM_001289937.1:c.2583T>C	NP_001276866.1:p.Ile861=
NM_004448.3:c.2583T>C , LRG_724t2:c.2583T>C	NP_004439.2:p.Ile861=
NR_110535.1:n.2907T>C
XM_024450641.1:c.2721T>C	XP_024306409.1:p.Ile907=
XM_024450642.1:c.2676T>C	XP_024306410.1:p.Ile892=
XM_024450643.1:c.2631T>C	XP_024306411.1:p.Ile877=
NM_001005862.3:c.2493T>C	NP_001005862.1:p.Ile831=
NM_001289936.2:c.2538T>C	NP_001276865.1:p.Ile846=
NM_001289937.2:c.2583T>C	NP_001276866.1:p.Ile861=
NM_001382782.1:c.2493T>C	NP_001369711.1:p.Ile831=
NM_001382783.1:c.2493T>C	NP_001369712.1:p.Ile831=
NM_001382784.1:c.2700T>C	NP_001369713.1:p.Ile900=
NM_001382785.1:c.2685T>C	NP_001369714.1:p.Ile895=
NM_001382786.1:c.2664T>C	NP_001369715.1:p.Ile888=
NM_001382787.1:c.2658T>C	NP_001369716.1:p.Ile886=
NM_001382788.1:c.2613T>C	NP_001369717.1:p.Ile871=
NM_001382789.1:c.2604T>C	NP_001369718.1:p.Ile868=
NM_001382790.1:c.2580T>C	NP_001369719.1:p.Ile860=
NM_001382791.1:c.2574T>C	NP_001369720.1:p.Ile858=
NM_001382792.1:c.2547T>C	NP_001369721.1:p.Ile849=
NM_001382793.1:c.2541T>C	NP_001369722.1:p.Ile847=
NM_001382794.1:c.2541T>C	NP_001369723.1:p.Ile847=
NM_001382795.1:c.2535T>C	NP_001369724.1:p.Ile845=
NM_001382796.1:c.2583T>C	NP_001369725.1:p.Ile861=
NM_001382797.1:c.2484T>C	NP_001369726.1:p.Ile828=
NM_001382798.1:c.2494-189T>C	NP_001369727.1:n.2494-189T>C
NM_001382799.1:c.2403T>C	NP_001369728.1:p.Ile801=
NM_001382800.1:c.2397T>C	NP_001369729.1:p.Ile799=
NM_001382801.1:c.2446-189T>C	NP_001369730.1:n.2446-189T>C
NM_001382802.1:c.2325T>C	NP_001369731.1:p.Ile775=
NM_001382803.1:c.2541T>C	NP_001369732.1:p.Ile847=
NM_001382804.1:c.1755T>C	NP_001369733.1:p.Ile585=
NM_001382805.1:c.2208+1478T>C	NP_001369734.1:n.2208+1478T>C
NM_001382806.1:c.1545T>C	NP_001369735.1:p.Ile515=
NM_004448.4:c.2583T>C MANE Select	NP_004439.2:p.Ile861=
NR_110535.2:n.2821T>C