Canonical Allele Identifier: CA399302836

Gene: ERBB2

Linked Data

• dbSNP Id: rs2145847358
• MyVariant Identifiers: chr17:g.37880994G>T (hg19) ; chr17:g.39724741G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39724741G>T , CM000679.2:g.39724741G>T	GRCh38
NC_000017.10:g.37880994G>T , CM000679.1:g.37880994G>T	GRCh37
NC_000017.9:g.35134520G>T	NCBI36
NG_007503.1:g.41602G>T , LRG_724:g.41602G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000269571.10:c.2323G>T MANE Select	ENSP00000269571.4:p.Ala775Ser
ENST00000269571.9:c.2323G>T	ENSP00000269571.4:p.Ala775Ser
ENST00000406381.6:c.2233G>T	ENSP00000385185.2:p.Ala745Ser
ENST00000445658.6:c.1495G>T	ENSP00000404047.2:p.Ala499Ser
ENST00000541774.5:c.2278G>T	ENSP00000446466.1:p.Ala760Ser
ENST00000578373.5:c.*2113G>T	ENSP00000463427.1:n.*2113G>T
ENST00000580074.1:c.429G>T
ENST00000583038.5:n.3457G>T
ENST00000584450.5:c.2323G>T	ENSP00000463714.1:p.Ala775Ser
ENST00000584601.5:c.2233G>T	ENSP00000462438.1:p.Ala745Ser
NM_001005862.2:c.2233G>T , LRG_724t1:c.2233G>T	NP_001005862.1:p.Ala745Ser
NM_001289936.1:c.2278G>T , LRG_724t4:c.2278G>T	NP_001276865.1:p.Ala760Ser
NM_001289937.1:c.2323G>T	NP_001276866.1:p.Ala775Ser
NM_004448.3:c.2323G>T , LRG_724t2:c.2323G>T	NP_004439.2:p.Ala775Ser
NR_110535.1:n.2647G>T
XM_024450641.1:c.2461G>T	XP_024306409.1:p.Ala821Ser
XM_024450642.1:c.2416G>T	XP_024306410.1:p.Ala806Ser
XM_024450643.1:c.2371G>T	XP_024306411.1:p.Ala791Ser
NM_001005862.3:c.2233G>T	NP_001005862.1:p.Ala745Ser
NM_001289936.2:c.2278G>T	NP_001276865.1:p.Ala760Ser
NM_001289937.2:c.2323G>T	NP_001276866.1:p.Ala775Ser
NM_001382782.1:c.2233G>T	NP_001369711.1:p.Ala745Ser
NM_001382783.1:c.2233G>T	NP_001369712.1:p.Ala745Ser
NM_001382784.1:c.2440G>T	NP_001369713.1:p.Ala814Ser
NM_001382785.1:c.2425G>T	NP_001369714.1:p.Ala809Ser
NM_001382786.1:c.2404G>T	NP_001369715.1:p.Ala802Ser
NM_001382787.1:c.2398G>T	NP_001369716.1:p.Ala800Ser
NM_001382788.1:c.2353G>T	NP_001369717.1:p.Ala785Ser
NM_001382789.1:c.2344G>T	NP_001369718.1:p.Ala782Ser
NM_001382790.1:c.2320G>T	NP_001369719.1:p.Ala774Ser
NM_001382791.1:c.2314G>T	NP_001369720.1:p.Ala772Ser
NM_001382792.1:c.2287G>T	NP_001369721.1:p.Ala763Ser
NM_001382793.1:c.2281G>T	NP_001369722.1:p.Ala761Ser
NM_001382794.1:c.2281G>T	NP_001369723.1:p.Ala761Ser
NM_001382795.1:c.2275G>T	NP_001369724.1:p.Ala759Ser
NM_001382796.1:c.2323G>T	NP_001369725.1:p.Ala775Ser
NM_001382797.1:c.2224G>T	NP_001369726.1:p.Ala742Ser
NM_001382798.1:c.2323G>T	NP_001369727.1:p.Ala775Ser
NM_001382799.1:c.2143G>T	NP_001369728.1:p.Ala715Ser
NM_001382800.1:c.2308-308G>T	NP_001369729.1:n.2308-308G>T
NM_001382801.1:c.2275G>T	NP_001369730.1:p.Ala759Ser
NM_001382802.1:c.2065G>T	NP_001369731.1:p.Ala689Ser
NM_001382803.1:c.2281G>T	NP_001369732.1:p.Ala761Ser
NM_001382804.1:c.1495G>T	NP_001369733.1:p.Ala499Ser
NM_001382805.1:c.2208+1081G>T	NP_001369734.1:n.2208+1081G>T
NM_001382806.1:c.1285G>T	NP_001369735.1:p.Ala429Ser
NM_004448.4:c.2323G>T MANE Select	NP_004439.2:p.Ala775Ser
NR_110535.2:n.2561G>T