Canonical Allele Identifier: CA2259227990
Gene: ERBB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39724750G= , CM000679.2:g.39724750G= GRCh38
NC_000017.10:g.37881003G= , CM000679.1:g.37881003G= GRCh37
NC_000017.9:g.35134529G= NCBI36
NG_007503.1:g.41611G= , LRG_724:g.41611G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000269571.10:c.2332G= MANE Select ENSP00000269571.4:p.Gly778=
ENST00000269571.9:c.2332G= ENSP00000269571.4:p.Gly778=
ENST00000406381.6:c.2242G= ENSP00000385185.2:p.Gly748=
ENST00000445658.6:c.1504G= ENSP00000404047.2:p.Gly502=
ENST00000541774.5:c.2287G= ENSP00000446466.1:p.Gly763=
ENST00000578373.5:c.*2122G= ENSP00000463427.1:n.*2122G=
ENST00000580074.1:c.438G=
ENST00000583038.5:n.3466G=
ENST00000584450.5:c.2332G= ENSP00000463714.1:p.Gly778=
ENST00000584601.5:c.2242G= ENSP00000462438.1:p.Gly748=
NM_001005862.2:c.2242G= , LRG_724t1:c.2242G= NP_001005862.1:p.Gly748=
NM_001289936.1:c.2287G= , LRG_724t4:c.2287G= NP_001276865.1:p.Gly763=
NM_001289937.1:c.2332G= NP_001276866.1:p.Gly778=
NM_004448.3:c.2332G= , LRG_724t2:c.2332G= NP_004439.2:p.Gly778=
NR_110535.1:n.2656G=
XM_024450641.1:c.2470G= XP_024306409.1:p.Gly824=
XM_024450642.1:c.2425G= XP_024306410.1:p.Gly809=
XM_024450643.1:c.2380G= XP_024306411.1:p.Gly794=
NM_001005862.3:c.2242G= NP_001005862.1:p.Gly748=
NM_001289936.2:c.2287G= NP_001276865.1:p.Gly763=
NM_001289937.2:c.2332G= NP_001276866.1:p.Gly778=
NM_001382782.1:c.2242G= NP_001369711.1:p.Gly748=
NM_001382783.1:c.2242G= NP_001369712.1:p.Gly748=
NM_001382784.1:c.2449G= NP_001369713.1:p.Gly817=
NM_001382785.1:c.2434G= NP_001369714.1:p.Gly812=
NM_001382786.1:c.2413G= NP_001369715.1:p.Gly805=
NM_001382787.1:c.2407G= NP_001369716.1:p.Gly803=
NM_001382788.1:c.2362G= NP_001369717.1:p.Gly788=
NM_001382789.1:c.2353G= NP_001369718.1:p.Gly785=
NM_001382790.1:c.2329G= NP_001369719.1:p.Gly777=
NM_001382791.1:c.2323G= NP_001369720.1:p.Gly775=
NM_001382792.1:c.2296G= NP_001369721.1:p.Gly766=
NM_001382793.1:c.2290G= NP_001369722.1:p.Gly764=
NM_001382794.1:c.2290G= NP_001369723.1:p.Gly764=
NM_001382795.1:c.2284G= NP_001369724.1:p.Gly762=
NM_001382796.1:c.2332G= NP_001369725.1:p.Gly778=
NM_001382797.1:c.2233G= NP_001369726.1:p.Gly745=
NM_001382798.1:c.2332G= NP_001369727.1:p.Gly778=
NM_001382799.1:c.2152G= NP_001369728.1:p.Gly718=
NM_001382800.1:c.2308-299G= NP_001369729.1:n.2308-299G=
NM_001382801.1:c.2284G= NP_001369730.1:p.Gly762=
NM_001382802.1:c.2074G= NP_001369731.1:p.Gly692=
NM_001382803.1:c.2290G= NP_001369732.1:p.Gly764=
NM_001382804.1:c.1504G= NP_001369733.1:p.Gly502=
NM_001382805.1:c.2208+1090G= NP_001369734.1:n.2208+1090G=
NM_001382806.1:c.1294G= NP_001369735.1:p.Gly432=
NM_004448.4:c.2332G= MANE Select NP_004439.2:p.Gly778=
NR_110535.2:n.2570G=