Canonical Allele Identifier: CA399303103

Gene: ERBB2

Linked Data

• dbSNP Id: rs2145849591
• MyVariant Identifiers: chr17:g.37881043C>T (hg19) ; chr17:g.39724790C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39724790C>T , CM000679.2:g.39724790C>T	GRCh38
NC_000017.10:g.37881043C>T , CM000679.1:g.37881043C>T	GRCh37
NC_000017.9:g.35134569C>T	NCBI36
NG_007503.1:g.41651C>T , LRG_724:g.41651C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.2372C>T MANE Select	ENSP00000269571.4:p.Thr791Ile
ENST00000269571.9:c.2372C>T	ENSP00000269571.4:p.Thr791Ile
ENST00000406381.6:c.2282C>T	ENSP00000385185.2:p.Thr761Ile
ENST00000445658.6:c.1544C>T	ENSP00000404047.2:p.Thr515Ile
ENST00000541774.5:c.2327C>T	ENSP00000446466.1:p.Thr776Ile
ENST00000578373.5:c.*2162C>T	ENSP00000463427.1:n.*2162C>T
ENST00000580074.1:c.478C>T
ENST00000583038.5:n.3506C>T
ENST00000584450.5:c.2372C>T	ENSP00000463714.1:p.Thr791Ile
ENST00000584601.5:c.2282C>T	ENSP00000462438.1:p.Thr761Ile
NM_001005862.2:c.2282C>T , LRG_724t1:c.2282C>T	NP_001005862.1:p.Thr761Ile
NM_001289936.1:c.2327C>T , LRG_724t4:c.2327C>T	NP_001276865.1:p.Thr776Ile
NM_001289937.1:c.2372C>T	NP_001276866.1:p.Thr791Ile
NM_004448.3:c.2372C>T , LRG_724t2:c.2372C>T	NP_004439.2:p.Thr791Ile
NR_110535.1:n.2696C>T
XM_024450641.1:c.2510C>T	XP_024306409.1:p.Thr837Ile
XM_024450642.1:c.2465C>T	XP_024306410.1:p.Thr822Ile
XM_024450643.1:c.2420C>T	XP_024306411.1:p.Thr807Ile
NM_001005862.3:c.2282C>T	NP_001005862.1:p.Thr761Ile
NM_001289936.2:c.2327C>T	NP_001276865.1:p.Thr776Ile
NM_001289937.2:c.2372C>T	NP_001276866.1:p.Thr791Ile
NM_001382782.1:c.2282C>T	NP_001369711.1:p.Thr761Ile
NM_001382783.1:c.2282C>T	NP_001369712.1:p.Thr761Ile
NM_001382784.1:c.2489C>T	NP_001369713.1:p.Thr830Ile
NM_001382785.1:c.2474C>T	NP_001369714.1:p.Thr825Ile
NM_001382786.1:c.2453C>T	NP_001369715.1:p.Thr818Ile
NM_001382787.1:c.2447C>T	NP_001369716.1:p.Thr816Ile
NM_001382788.1:c.2402C>T	NP_001369717.1:p.Thr801Ile
NM_001382789.1:c.2393C>T	NP_001369718.1:p.Thr798Ile
NM_001382790.1:c.2369C>T	NP_001369719.1:p.Thr790Ile
NM_001382791.1:c.2363C>T	NP_001369720.1:p.Thr788Ile
NM_001382792.1:c.2336C>T	NP_001369721.1:p.Thr779Ile
NM_001382793.1:c.2330C>T	NP_001369722.1:p.Thr777Ile
NM_001382794.1:c.2330C>T	NP_001369723.1:p.Thr777Ile
NM_001382795.1:c.2324C>T	NP_001369724.1:p.Thr775Ile
NM_001382796.1:c.2372C>T	NP_001369725.1:p.Thr791Ile
NM_001382797.1:c.2273C>T	NP_001369726.1:p.Thr758Ile
NM_001382798.1:c.2372C>T	NP_001369727.1:p.Thr791Ile
NM_001382799.1:c.2192C>T	NP_001369728.1:p.Thr731Ile
NM_001382800.1:c.2308-259C>T	NP_001369729.1:n.2308-259C>T
NM_001382801.1:c.2324C>T	NP_001369730.1:p.Thr775Ile
NM_001382802.1:c.2114C>T	NP_001369731.1:p.Thr705Ile
NM_001382803.1:c.2330C>T	NP_001369732.1:p.Thr777Ile
NM_001382804.1:c.1544C>T	NP_001369733.1:p.Thr515Ile
NM_001382805.1:c.2208+1130C>T	NP_001369734.1:n.2208+1130C>T
NM_001382806.1:c.1334C>T	NP_001369735.1:p.Thr445Ile
NM_004448.4:c.2372C>T MANE Select	NP_004439.2:p.Thr791Ile
NR_110535.2:n.2610C>T