Canonical Allele Identifier: CA399302820

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37880991A>C (hg19) ; chr17:g.39724738A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39724738A>C , CM000679.2:g.39724738A>C	GRCh38
NC_000017.10:g.37880991A>C , CM000679.1:g.37880991A>C	GRCh37
NC_000017.9:g.35134517A>C	NCBI36
NG_007503.1:g.41599A>C , LRG_724:g.41599A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000269571.10:c.2320A>C MANE Select	ENSP00000269571.4:p.Met774Leu
ENST00000269571.9:c.2320A>C	ENSP00000269571.4:p.Met774Leu
ENST00000406381.6:c.2230A>C	ENSP00000385185.2:p.Met744Leu
ENST00000445658.6:c.1492A>C	ENSP00000404047.2:p.Met498Leu
ENST00000541774.5:c.2275A>C	ENSP00000446466.1:p.Met759Leu
ENST00000578373.5:c.*2110A>C	ENSP00000463427.1:n.*2110A>C
ENST00000580074.1:c.426A>C
ENST00000583038.5:n.3454A>C
ENST00000584450.5:c.2320A>C	ENSP00000463714.1:p.Met774Leu
ENST00000584601.5:c.2230A>C	ENSP00000462438.1:p.Met744Leu
NM_001005862.2:c.2230A>C , LRG_724t1:c.2230A>C	NP_001005862.1:p.Met744Leu
NM_001289936.1:c.2275A>C , LRG_724t4:c.2275A>C	NP_001276865.1:p.Met759Leu
NM_001289937.1:c.2320A>C	NP_001276866.1:p.Met774Leu
NM_004448.3:c.2320A>C , LRG_724t2:c.2320A>C	NP_004439.2:p.Met774Leu
NR_110535.1:n.2644A>C
XM_024450641.1:c.2458A>C	XP_024306409.1:p.Met820Leu
XM_024450642.1:c.2413A>C	XP_024306410.1:p.Met805Leu
XM_024450643.1:c.2368A>C	XP_024306411.1:p.Met790Leu
NM_001005862.3:c.2230A>C	NP_001005862.1:p.Met744Leu
NM_001289936.2:c.2275A>C	NP_001276865.1:p.Met759Leu
NM_001289937.2:c.2320A>C	NP_001276866.1:p.Met774Leu
NM_001382782.1:c.2230A>C	NP_001369711.1:p.Met744Leu
NM_001382783.1:c.2230A>C	NP_001369712.1:p.Met744Leu
NM_001382784.1:c.2437A>C	NP_001369713.1:p.Met813Leu
NM_001382785.1:c.2422A>C	NP_001369714.1:p.Met808Leu
NM_001382786.1:c.2401A>C	NP_001369715.1:p.Met801Leu
NM_001382787.1:c.2395A>C	NP_001369716.1:p.Met799Leu
NM_001382788.1:c.2350A>C	NP_001369717.1:p.Met784Leu
NM_001382789.1:c.2341A>C	NP_001369718.1:p.Met781Leu
NM_001382790.1:c.2317A>C	NP_001369719.1:p.Met773Leu
NM_001382791.1:c.2311A>C	NP_001369720.1:p.Met771Leu
NM_001382792.1:c.2284A>C	NP_001369721.1:p.Met762Leu
NM_001382793.1:c.2278A>C	NP_001369722.1:p.Met760Leu
NM_001382794.1:c.2278A>C	NP_001369723.1:p.Met760Leu
NM_001382795.1:c.2272A>C	NP_001369724.1:p.Met758Leu
NM_001382796.1:c.2320A>C	NP_001369725.1:p.Met774Leu
NM_001382797.1:c.2221A>C	NP_001369726.1:p.Met741Leu
NM_001382798.1:c.2320A>C	NP_001369727.1:p.Met774Leu
NM_001382799.1:c.2140A>C	NP_001369728.1:p.Met714Leu
NM_001382800.1:c.2308-311A>C	NP_001369729.1:n.2308-311A>C
NM_001382801.1:c.2272A>C	NP_001369730.1:p.Met758Leu
NM_001382802.1:c.2062A>C	NP_001369731.1:p.Met688Leu
NM_001382803.1:c.2278A>C	NP_001369732.1:p.Met760Leu
NM_001382804.1:c.1492A>C	NP_001369733.1:p.Met498Leu
NM_001382805.1:c.2208+1078A>C	NP_001369734.1:n.2208+1078A>C
NM_001382806.1:c.1282A>C	NP_001369735.1:p.Met428Leu
NM_004448.4:c.2320A>C MANE Select	NP_004439.2:p.Met774Leu
NR_110535.2:n.2558A>C