Canonical Allele Identifier: CA399304425

Gene: ERBB2

Linked Data

• gnomAD v4: 17-39725100-C-T
• MyVariant Identifiers: chr17:g.37881353C>T (hg19) ; chr17:g.39725100C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39725100C>T , CM000679.2:g.39725100C>T	GRCh38
NC_000017.10:g.37881353C>T , CM000679.1:g.37881353C>T	GRCh37
NC_000017.9:g.35134879C>T	NCBI36
NG_007503.1:g.41961C>T , LRG_724:g.41961C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.2545C>T MANE Select	ENSP00000269571.4:p.Arg849Trp
ENST00000269571.9:c.2545C>T	ENSP00000269571.4:p.Arg849Trp
ENST00000406381.6:c.2455C>T	ENSP00000385185.2:p.Arg819Trp
ENST00000445658.6:c.1717C>T	ENSP00000404047.2:p.Arg573Trp
ENST00000541774.5:c.2500C>T	ENSP00000446466.1:p.Arg834Trp
ENST00000578373.5:c.*2335C>T	ENSP00000463427.1:n.*2335C>T
ENST00000580074.1:c.651C>T
ENST00000583038.5:n.3679C>T
ENST00000584450.5:c.2545C>T	ENSP00000463714.1:p.Arg849Trp
ENST00000584601.5:c.2455C>T	ENSP00000462438.1:p.Arg819Trp
NM_001005862.2:c.2455C>T , LRG_724t1:c.2455C>T	NP_001005862.1:p.Arg819Trp
NM_001289936.1:c.2500C>T , LRG_724t4:c.2500C>T	NP_001276865.1:p.Arg834Trp
NM_001289937.1:c.2545C>T	NP_001276866.1:p.Arg849Trp
NM_004448.3:c.2545C>T , LRG_724t2:c.2545C>T	NP_004439.2:p.Arg849Trp
NR_110535.1:n.2869C>T
XM_024450641.1:c.2683C>T	XP_024306409.1:p.Arg895Trp
XM_024450642.1:c.2638C>T	XP_024306410.1:p.Arg880Trp
XM_024450643.1:c.2593C>T	XP_024306411.1:p.Arg865Trp
NM_001005862.3:c.2455C>T	NP_001005862.1:p.Arg819Trp
NM_001289936.2:c.2500C>T	NP_001276865.1:p.Arg834Trp
NM_001289937.2:c.2545C>T	NP_001276866.1:p.Arg849Trp
NM_001382782.1:c.2455C>T	NP_001369711.1:p.Arg819Trp
NM_001382783.1:c.2455C>T	NP_001369712.1:p.Arg819Trp
NM_001382784.1:c.2662C>T	NP_001369713.1:p.Arg888Trp
NM_001382785.1:c.2647C>T	NP_001369714.1:p.Arg883Trp
NM_001382786.1:c.2626C>T	NP_001369715.1:p.Arg876Trp
NM_001382787.1:c.2620C>T	NP_001369716.1:p.Arg874Trp
NM_001382788.1:c.2575C>T	NP_001369717.1:p.Arg859Trp
NM_001382789.1:c.2566C>T	NP_001369718.1:p.Arg856Trp
NM_001382790.1:c.2542C>T	NP_001369719.1:p.Arg848Trp
NM_001382791.1:c.2536C>T	NP_001369720.1:p.Arg846Trp
NM_001382792.1:c.2509C>T	NP_001369721.1:p.Arg837Trp
NM_001382793.1:c.2503C>T	NP_001369722.1:p.Arg835Trp
NM_001382794.1:c.2503C>T	NP_001369723.1:p.Arg835Trp
NM_001382795.1:c.2497C>T	NP_001369724.1:p.Arg833Trp
NM_001382796.1:c.2545C>T	NP_001369725.1:p.Arg849Trp
NM_001382797.1:c.2446C>T	NP_001369726.1:p.Arg816Trp
NM_001382798.1:c.2493+189C>T	NP_001369727.1:n.2493+189C>T
NM_001382799.1:c.2365C>T	NP_001369728.1:p.Arg789Trp
NM_001382800.1:c.2359C>T	NP_001369729.1:p.Arg787Trp
NM_001382801.1:c.2445+189C>T	NP_001369730.1:n.2445+189C>T
NM_001382802.1:c.2287C>T	NP_001369731.1:p.Arg763Trp
NM_001382803.1:c.2503C>T	NP_001369732.1:p.Arg835Trp
NM_001382804.1:c.1717C>T	NP_001369733.1:p.Arg573Trp
NM_001382805.1:c.2208+1440C>T	NP_001369734.1:n.2208+1440C>T
NM_001382806.1:c.1507C>T	NP_001369735.1:p.Arg503Trp
NM_004448.4:c.2545C>T MANE Select	NP_004439.2:p.Arg849Trp
NR_110535.2:n.2783C>T