Canonical Allele Identifier: CA399303093

Gene: ERBB2

Linked Data

• dbSNP Id: rs2145849536
• MyVariant Identifiers: chr17:g.37881042A>T (hg19) ; chr17:g.39724789A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39724789A>T , CM000679.2:g.39724789A>T	GRCh38
NC_000017.10:g.37881042A>T , CM000679.1:g.37881042A>T	GRCh37
NC_000017.9:g.35134568A>T	NCBI36
NG_007503.1:g.41650A>T , LRG_724:g.41650A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.2371A>T MANE Select	ENSP00000269571.4:p.Thr791Ser
ENST00000269571.9:c.2371A>T	ENSP00000269571.4:p.Thr791Ser
ENST00000406381.6:c.2281A>T	ENSP00000385185.2:p.Thr761Ser
ENST00000445658.6:c.1543A>T	ENSP00000404047.2:p.Thr515Ser
ENST00000541774.5:c.2326A>T	ENSP00000446466.1:p.Thr776Ser
ENST00000578373.5:c.*2161A>T	ENSP00000463427.1:n.*2161A>T
ENST00000580074.1:c.477A>T
ENST00000583038.5:n.3505A>T
ENST00000584450.5:c.2371A>T	ENSP00000463714.1:p.Thr791Ser
ENST00000584601.5:c.2281A>T	ENSP00000462438.1:p.Thr761Ser
NM_001005862.2:c.2281A>T , LRG_724t1:c.2281A>T	NP_001005862.1:p.Thr761Ser
NM_001289936.1:c.2326A>T , LRG_724t4:c.2326A>T	NP_001276865.1:p.Thr776Ser
NM_001289937.1:c.2371A>T	NP_001276866.1:p.Thr791Ser
NM_004448.3:c.2371A>T , LRG_724t2:c.2371A>T	NP_004439.2:p.Thr791Ser
NR_110535.1:n.2695A>T
XM_024450641.1:c.2509A>T	XP_024306409.1:p.Thr837Ser
XM_024450642.1:c.2464A>T	XP_024306410.1:p.Thr822Ser
XM_024450643.1:c.2419A>T	XP_024306411.1:p.Thr807Ser
NM_001005862.3:c.2281A>T	NP_001005862.1:p.Thr761Ser
NM_001289936.2:c.2326A>T	NP_001276865.1:p.Thr776Ser
NM_001289937.2:c.2371A>T	NP_001276866.1:p.Thr791Ser
NM_001382782.1:c.2281A>T	NP_001369711.1:p.Thr761Ser
NM_001382783.1:c.2281A>T	NP_001369712.1:p.Thr761Ser
NM_001382784.1:c.2488A>T	NP_001369713.1:p.Thr830Ser
NM_001382785.1:c.2473A>T	NP_001369714.1:p.Thr825Ser
NM_001382786.1:c.2452A>T	NP_001369715.1:p.Thr818Ser
NM_001382787.1:c.2446A>T	NP_001369716.1:p.Thr816Ser
NM_001382788.1:c.2401A>T	NP_001369717.1:p.Thr801Ser
NM_001382789.1:c.2392A>T	NP_001369718.1:p.Thr798Ser
NM_001382790.1:c.2368A>T	NP_001369719.1:p.Thr790Ser
NM_001382791.1:c.2362A>T	NP_001369720.1:p.Thr788Ser
NM_001382792.1:c.2335A>T	NP_001369721.1:p.Thr779Ser
NM_001382793.1:c.2329A>T	NP_001369722.1:p.Thr777Ser
NM_001382794.1:c.2329A>T	NP_001369723.1:p.Thr777Ser
NM_001382795.1:c.2323A>T	NP_001369724.1:p.Thr775Ser
NM_001382796.1:c.2371A>T	NP_001369725.1:p.Thr791Ser
NM_001382797.1:c.2272A>T	NP_001369726.1:p.Thr758Ser
NM_001382798.1:c.2371A>T	NP_001369727.1:p.Thr791Ser
NM_001382799.1:c.2191A>T	NP_001369728.1:p.Thr731Ser
NM_001382800.1:c.2308-260A>T	NP_001369729.1:n.2308-260A>T
NM_001382801.1:c.2323A>T	NP_001369730.1:p.Thr775Ser
NM_001382802.1:c.2113A>T	NP_001369731.1:p.Thr705Ser
NM_001382803.1:c.2329A>T	NP_001369732.1:p.Thr777Ser
NM_001382804.1:c.1543A>T	NP_001369733.1:p.Thr515Ser
NM_001382805.1:c.2208+1129A>T	NP_001369734.1:n.2208+1129A>T
NM_001382806.1:c.1333A>T	NP_001369735.1:p.Thr445Ser
NM_004448.4:c.2371A>T MANE Select	NP_004439.2:p.Thr791Ser
NR_110535.2:n.2609A>T