Canonical Allele Identifier: CA399302830

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37880993G>C (hg19) ; chr17:g.39724740G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39724740G>C , CM000679.2:g.39724740G>C	GRCh38
NC_000017.10:g.37880993G>C , CM000679.1:g.37880993G>C	GRCh37
NC_000017.9:g.35134519G>C	NCBI36
NG_007503.1:g.41601G>C , LRG_724:g.41601G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.2322G>C MANE Select	ENSP00000269571.4:p.Met774Ile
ENST00000269571.9:c.2322G>C	ENSP00000269571.4:p.Met774Ile
ENST00000406381.6:c.2232G>C	ENSP00000385185.2:p.Met744Ile
ENST00000445658.6:c.1494G>C	ENSP00000404047.2:p.Met498Ile
ENST00000541774.5:c.2277G>C	ENSP00000446466.1:p.Met759Ile
ENST00000578373.5:c.*2112G>C	ENSP00000463427.1:n.*2112G>C
ENST00000580074.1:c.428G>C
ENST00000583038.5:n.3456G>C
ENST00000584450.5:c.2322G>C	ENSP00000463714.1:p.Met774Ile
ENST00000584601.5:c.2232G>C	ENSP00000462438.1:p.Met744Ile
NM_001005862.2:c.2232G>C , LRG_724t1:c.2232G>C	NP_001005862.1:p.Met744Ile
NM_001289936.1:c.2277G>C , LRG_724t4:c.2277G>C	NP_001276865.1:p.Met759Ile
NM_001289937.1:c.2322G>C	NP_001276866.1:p.Met774Ile
NM_004448.3:c.2322G>C , LRG_724t2:c.2322G>C	NP_004439.2:p.Met774Ile
NR_110535.1:n.2646G>C
XM_024450641.1:c.2460G>C	XP_024306409.1:p.Met820Ile
XM_024450642.1:c.2415G>C	XP_024306410.1:p.Met805Ile
XM_024450643.1:c.2370G>C	XP_024306411.1:p.Met790Ile
NM_001005862.3:c.2232G>C	NP_001005862.1:p.Met744Ile
NM_001289936.2:c.2277G>C	NP_001276865.1:p.Met759Ile
NM_001289937.2:c.2322G>C	NP_001276866.1:p.Met774Ile
NM_001382782.1:c.2232G>C	NP_001369711.1:p.Met744Ile
NM_001382783.1:c.2232G>C	NP_001369712.1:p.Met744Ile
NM_001382784.1:c.2439G>C	NP_001369713.1:p.Met813Ile
NM_001382785.1:c.2424G>C	NP_001369714.1:p.Met808Ile
NM_001382786.1:c.2403G>C	NP_001369715.1:p.Met801Ile
NM_001382787.1:c.2397G>C	NP_001369716.1:p.Met799Ile
NM_001382788.1:c.2352G>C	NP_001369717.1:p.Met784Ile
NM_001382789.1:c.2343G>C	NP_001369718.1:p.Met781Ile
NM_001382790.1:c.2319G>C	NP_001369719.1:p.Met773Ile
NM_001382791.1:c.2313G>C	NP_001369720.1:p.Met771Ile
NM_001382792.1:c.2286G>C	NP_001369721.1:p.Met762Ile
NM_001382793.1:c.2280G>C	NP_001369722.1:p.Met760Ile
NM_001382794.1:c.2280G>C	NP_001369723.1:p.Met760Ile
NM_001382795.1:c.2274G>C	NP_001369724.1:p.Met758Ile
NM_001382796.1:c.2322G>C	NP_001369725.1:p.Met774Ile
NM_001382797.1:c.2223G>C	NP_001369726.1:p.Met741Ile
NM_001382798.1:c.2322G>C	NP_001369727.1:p.Met774Ile
NM_001382799.1:c.2142G>C	NP_001369728.1:p.Met714Ile
NM_001382800.1:c.2308-309G>C	NP_001369729.1:n.2308-309G>C
NM_001382801.1:c.2274G>C	NP_001369730.1:p.Met758Ile
NM_001382802.1:c.2064G>C	NP_001369731.1:p.Met688Ile
NM_001382803.1:c.2280G>C	NP_001369732.1:p.Met760Ile
NM_001382804.1:c.1494G>C	NP_001369733.1:p.Met498Ile
NM_001382805.1:c.2208+1080G>C	NP_001369734.1:n.2208+1080G>C
NM_001382806.1:c.1284G>C	NP_001369735.1:p.Met428Ile
NM_004448.4:c.2322G>C MANE Select	NP_004439.2:p.Met774Ile
NR_110535.2:n.2560G>C