Canonical Allele Identifier: CA499670871

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37881035C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39724782C>A , CM000679.2:g.39724782C>A	GRCh38
NC_000017.10:g.37881035C>A , CM000679.1:g.37881035C>A	GRCh37
NC_000017.9:g.35134561C>A	NCBI36
NG_007503.1:g.41643C>A , LRG_724:g.41643C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.2364C>A MANE Select	ENSP00000269571.4:p.Ile788=
ENST00000269571.9:c.2364C>A	ENSP00000269571.4:p.Ile788=
ENST00000406381.6:c.2274C>A	ENSP00000385185.2:p.Ile758=
ENST00000445658.6:c.1536C>A	ENSP00000404047.2:p.Ile512=
ENST00000541774.5:c.2319C>A	ENSP00000446466.1:p.Ile773=
ENST00000578373.5:c.*2154C>A	ENSP00000463427.1:n.*2154C>A
ENST00000580074.1:c.470C>A
ENST00000583038.5:n.3498C>A
ENST00000584450.5:c.2364C>A	ENSP00000463714.1:p.Ile788=
ENST00000584601.5:c.2274C>A	ENSP00000462438.1:p.Ile758=
NM_001005862.2:c.2274C>A , LRG_724t1:c.2274C>A	NP_001005862.1:p.Ile758=
NM_001289936.1:c.2319C>A , LRG_724t4:c.2319C>A	NP_001276865.1:p.Ile773=
NM_001289937.1:c.2364C>A	NP_001276866.1:p.Ile788=
NM_004448.3:c.2364C>A , LRG_724t2:c.2364C>A	NP_004439.2:p.Ile788=
NR_110535.1:n.2688C>A
XM_024450641.1:c.2502C>A	XP_024306409.1:p.Ile834=
XM_024450642.1:c.2457C>A	XP_024306410.1:p.Ile819=
XM_024450643.1:c.2412C>A	XP_024306411.1:p.Ile804=
NM_001005862.3:c.2274C>A	NP_001005862.1:p.Ile758=
NM_001289936.2:c.2319C>A	NP_001276865.1:p.Ile773=
NM_001289937.2:c.2364C>A	NP_001276866.1:p.Ile788=
NM_001382782.1:c.2274C>A	NP_001369711.1:p.Ile758=
NM_001382783.1:c.2274C>A	NP_001369712.1:p.Ile758=
NM_001382784.1:c.2481C>A	NP_001369713.1:p.Ile827=
NM_001382785.1:c.2466C>A	NP_001369714.1:p.Ile822=
NM_001382786.1:c.2445C>A	NP_001369715.1:p.Ile815=
NM_001382787.1:c.2439C>A	NP_001369716.1:p.Ile813=
NM_001382788.1:c.2394C>A	NP_001369717.1:p.Ile798=
NM_001382789.1:c.2385C>A	NP_001369718.1:p.Ile795=
NM_001382790.1:c.2361C>A	NP_001369719.1:p.Ile787=
NM_001382791.1:c.2355C>A	NP_001369720.1:p.Ile785=
NM_001382792.1:c.2328C>A	NP_001369721.1:p.Ile776=
NM_001382793.1:c.2322C>A	NP_001369722.1:p.Ile774=
NM_001382794.1:c.2322C>A	NP_001369723.1:p.Ile774=
NM_001382795.1:c.2316C>A	NP_001369724.1:p.Ile772=
NM_001382796.1:c.2364C>A	NP_001369725.1:p.Ile788=
NM_001382797.1:c.2265C>A	NP_001369726.1:p.Ile755=
NM_001382798.1:c.2364C>A	NP_001369727.1:p.Ile788=
NM_001382799.1:c.2184C>A	NP_001369728.1:p.Ile728=
NM_001382800.1:c.2308-267C>A	NP_001369729.1:n.2308-267C>A
NM_001382801.1:c.2316C>A	NP_001369730.1:p.Ile772=
NM_001382802.1:c.2106C>A	NP_001369731.1:p.Ile702=
NM_001382803.1:c.2322C>A	NP_001369732.1:p.Ile774=
NM_001382804.1:c.1536C>A	NP_001369733.1:p.Ile512=
NM_001382805.1:c.2208+1122C>A	NP_001369734.1:n.2208+1122C>A
NM_001382806.1:c.1326C>A	NP_001369735.1:p.Ile442=
NM_004448.4:c.2364C>A MANE Select	NP_004439.2:p.Ile788=
NR_110535.2:n.2602C>A