Canonical Allele Identifier: CA399303298

Gene: ERBB2

Linked Data

• dbSNP Id: rs2145850754
• MyVariant Identifiers: chr17:g.37881073T>C (hg19) ; chr17:g.39724820T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39724820T>C , CM000679.2:g.39724820T>C	GRCh38
NC_000017.10:g.37881073T>C , CM000679.1:g.37881073T>C	GRCh37
NC_000017.9:g.35134599T>C	NCBI36
NG_007503.1:g.41681T>C , LRG_724:g.41681T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.2402T>C MANE Select	ENSP00000269571.4:p.Met801Thr
ENST00000269571.9:c.2402T>C	ENSP00000269571.4:p.Met801Thr
ENST00000406381.6:c.2312T>C	ENSP00000385185.2:p.Met771Thr
ENST00000445658.6:c.1574T>C	ENSP00000404047.2:p.Met525Thr
ENST00000541774.5:c.2357T>C	ENSP00000446466.1:p.Met786Thr
ENST00000578373.5:c.*2192T>C	ENSP00000463427.1:n.*2192T>C
ENST00000580074.1:c.508T>C
ENST00000583038.5:n.3536T>C
ENST00000584450.5:c.2402T>C	ENSP00000463714.1:p.Met801Thr
ENST00000584601.5:c.2312T>C	ENSP00000462438.1:p.Met771Thr
NM_001005862.2:c.2312T>C , LRG_724t1:c.2312T>C	NP_001005862.1:p.Met771Thr
NM_001289936.1:c.2357T>C , LRG_724t4:c.2357T>C	NP_001276865.1:p.Met786Thr
NM_001289937.1:c.2402T>C	NP_001276866.1:p.Met801Thr
NM_004448.3:c.2402T>C , LRG_724t2:c.2402T>C	NP_004439.2:p.Met801Thr
NR_110535.1:n.2726T>C
XM_024450641.1:c.2540T>C	XP_024306409.1:p.Met847Thr
XM_024450642.1:c.2495T>C	XP_024306410.1:p.Met832Thr
XM_024450643.1:c.2450T>C	XP_024306411.1:p.Met817Thr
NM_001005862.3:c.2312T>C	NP_001005862.1:p.Met771Thr
NM_001289936.2:c.2357T>C	NP_001276865.1:p.Met786Thr
NM_001289937.2:c.2402T>C	NP_001276866.1:p.Met801Thr
NM_001382782.1:c.2312T>C	NP_001369711.1:p.Met771Thr
NM_001382783.1:c.2312T>C	NP_001369712.1:p.Met771Thr
NM_001382784.1:c.2519T>C	NP_001369713.1:p.Met840Thr
NM_001382785.1:c.2504T>C	NP_001369714.1:p.Met835Thr
NM_001382786.1:c.2483T>C	NP_001369715.1:p.Met828Thr
NM_001382787.1:c.2477T>C	NP_001369716.1:p.Met826Thr
NM_001382788.1:c.2432T>C	NP_001369717.1:p.Met811Thr
NM_001382789.1:c.2423T>C	NP_001369718.1:p.Met808Thr
NM_001382790.1:c.2399T>C	NP_001369719.1:p.Met800Thr
NM_001382791.1:c.2393T>C	NP_001369720.1:p.Met798Thr
NM_001382792.1:c.2366T>C	NP_001369721.1:p.Met789Thr
NM_001382793.1:c.2360T>C	NP_001369722.1:p.Met787Thr
NM_001382794.1:c.2360T>C	NP_001369723.1:p.Met787Thr
NM_001382795.1:c.2354T>C	NP_001369724.1:p.Met785Thr
NM_001382796.1:c.2402T>C	NP_001369725.1:p.Met801Thr
NM_001382797.1:c.2303T>C	NP_001369726.1:p.Met768Thr
NM_001382798.1:c.2402T>C	NP_001369727.1:p.Met801Thr
NM_001382799.1:c.2222T>C	NP_001369728.1:p.Met741Thr
NM_001382800.1:c.2308-229T>C	NP_001369729.1:n.2308-229T>C
NM_001382801.1:c.2354T>C	NP_001369730.1:p.Met785Thr
NM_001382802.1:c.2144T>C	NP_001369731.1:p.Met715Thr
NM_001382803.1:c.2360T>C	NP_001369732.1:p.Met787Thr
NM_001382804.1:c.1574T>C	NP_001369733.1:p.Met525Thr
NM_001382805.1:c.2208+1160T>C	NP_001369734.1:n.2208+1160T>C
NM_001382806.1:c.1364T>C	NP_001369735.1:p.Met455Thr
NM_004448.4:c.2402T>C MANE Select	NP_004439.2:p.Met801Thr
NR_110535.2:n.2640T>C