Canonical Allele Identifier: CA399303214
Gene: ERBB2 HGNC NCBI

Linked Data

dbSNP Id: rs2145850231

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39724807G>A , CM000679.2:g.39724807G>A GRCh38
NC_000017.10:g.37881060G>A , CM000679.1:g.37881060G>A GRCh37
NC_000017.9:g.35134586G>A NCBI36
NG_007503.1:g.41668G>A , LRG_724:g.41668G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000269571.10:c.2389G>A MANE Select ENSP00000269571.4:p.Val797Met
ENST00000269571.9:c.2389G>A ENSP00000269571.4:p.Val797Met
ENST00000406381.6:c.2299G>A ENSP00000385185.2:p.Val767Met
ENST00000445658.6:c.1561G>A ENSP00000404047.2:p.Val521Met
ENST00000541774.5:c.2344G>A ENSP00000446466.1:p.Val782Met
ENST00000578373.5:c.*2179G>A ENSP00000463427.1:n.*2179G>A
ENST00000580074.1:c.495G>A
ENST00000583038.5:n.3523G>A
ENST00000584450.5:c.2389G>A ENSP00000463714.1:p.Val797Met
ENST00000584601.5:c.2299G>A ENSP00000462438.1:p.Val767Met
NM_001005862.2:c.2299G>A , LRG_724t1:c.2299G>A NP_001005862.1:p.Val767Met
NM_001289936.1:c.2344G>A , LRG_724t4:c.2344G>A NP_001276865.1:p.Val782Met
NM_001289937.1:c.2389G>A NP_001276866.1:p.Val797Met
NM_004448.3:c.2389G>A , LRG_724t2:c.2389G>A NP_004439.2:p.Val797Met
NR_110535.1:n.2713G>A
XM_024450641.1:c.2527G>A XP_024306409.1:p.Val843Met
XM_024450642.1:c.2482G>A XP_024306410.1:p.Val828Met
XM_024450643.1:c.2437G>A XP_024306411.1:p.Val813Met
NM_001005862.3:c.2299G>A NP_001005862.1:p.Val767Met
NM_001289936.2:c.2344G>A NP_001276865.1:p.Val782Met
NM_001289937.2:c.2389G>A NP_001276866.1:p.Val797Met
NM_001382782.1:c.2299G>A NP_001369711.1:p.Val767Met
NM_001382783.1:c.2299G>A NP_001369712.1:p.Val767Met
NM_001382784.1:c.2506G>A NP_001369713.1:p.Val836Met
NM_001382785.1:c.2491G>A NP_001369714.1:p.Val831Met
NM_001382786.1:c.2470G>A NP_001369715.1:p.Val824Met
NM_001382787.1:c.2464G>A NP_001369716.1:p.Val822Met
NM_001382788.1:c.2419G>A NP_001369717.1:p.Val807Met
NM_001382789.1:c.2410G>A NP_001369718.1:p.Val804Met
NM_001382790.1:c.2386G>A NP_001369719.1:p.Val796Met
NM_001382791.1:c.2380G>A NP_001369720.1:p.Val794Met
NM_001382792.1:c.2353G>A NP_001369721.1:p.Val785Met
NM_001382793.1:c.2347G>A NP_001369722.1:p.Val783Met
NM_001382794.1:c.2347G>A NP_001369723.1:p.Val783Met
NM_001382795.1:c.2341G>A NP_001369724.1:p.Val781Met
NM_001382796.1:c.2389G>A NP_001369725.1:p.Val797Met
NM_001382797.1:c.2290G>A NP_001369726.1:p.Val764Met
NM_001382798.1:c.2389G>A NP_001369727.1:p.Val797Met
NM_001382799.1:c.2209G>A NP_001369728.1:p.Val737Met
NM_001382800.1:c.2308-242G>A NP_001369729.1:n.2308-242G>A
NM_001382801.1:c.2341G>A NP_001369730.1:p.Val781Met
NM_001382802.1:c.2131G>A NP_001369731.1:p.Val711Met
NM_001382803.1:c.2347G>A NP_001369732.1:p.Val783Met
NM_001382804.1:c.1561G>A NP_001369733.1:p.Val521Met
NM_001382805.1:c.2208+1147G>A NP_001369734.1:n.2208+1147G>A
NM_001382806.1:c.1351G>A NP_001369735.1:p.Val451Met
NM_004448.4:c.2389G>A MANE Select NP_004439.2:p.Val797Met
NR_110535.2:n.2627G>A