Canonical Allele Identifier: CA399313572

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143302147
• MyVariant Identifiers: chr17:g.37884088T>G (hg19) ; chr17:g.39727835T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727835T>G , CM000679.2:g.39727835T>G	GRCh38
NC_000017.10:g.37884088T>G , CM000679.1:g.37884088T>G	GRCh37
NC_000017.9:g.35137614T>G	NCBI36
NG_007503.1:g.44696T>G , LRG_724:g.44696T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3559T>G MANE Select	ENSP00000269571.4:p.Phe1187Val
ENST00000269571.9:c.3559T>G	ENSP00000269571.4:p.Phe1187Val
ENST00000406381.6:c.3469T>G	ENSP00000385185.2:p.Phe1157Val
ENST00000445658.6:c.2731T>G	ENSP00000404047.2:p.Phe911Val
ENST00000541774.5:c.3514T>G	ENSP00000446466.1:p.Phe1172Val
ENST00000578373.5:c.*3349T>G	ENSP00000463427.1:n.*3349T>G
ENST00000584450.5:c.*138T>G	ENSP00000463714.1:n.*138T>G
ENST00000584601.5:c.3469T>G	ENSP00000462438.1:p.Phe1157Val
NM_001005862.2:c.3469T>G , LRG_724t1:c.3469T>G	NP_001005862.1:p.Phe1157Val
NM_001289936.1:c.3514T>G , LRG_724t4:c.3514T>G	NP_001276865.1:p.Phe1172Val
NM_001289937.1:c.*138T>G	NP_001276866.1:n.*138T>G
NM_004448.3:c.3559T>G , LRG_724t2:c.3559T>G	NP_004439.2:p.Phe1187Val
NR_110535.1:n.3883T>G
XM_024450641.1:c.3697T>G	XP_024306409.1:p.Phe1233Val
XM_024450642.1:c.3652T>G	XP_024306410.1:p.Phe1218Val
XM_024450643.1:c.3607T>G	XP_024306411.1:p.Phe1203Val
NM_001005862.3:c.3469T>G	NP_001005862.1:p.Phe1157Val
NM_001289936.2:c.3514T>G	NP_001276865.1:p.Phe1172Val
NM_001289937.2:c.*138T>G	NP_001276866.1:n.*138T>G
NM_001382782.1:c.3469T>G	NP_001369711.1:p.Phe1157Val
NM_001382783.1:c.3469T>G	NP_001369712.1:p.Phe1157Val
NM_001382784.1:c.3676T>G	NP_001369713.1:p.Phe1226Val
NM_001382785.1:c.3661T>G	NP_001369714.1:p.Phe1221Val
NM_001382786.1:c.3640T>G	NP_001369715.1:p.Phe1214Val
NM_001382787.1:c.3634T>G	NP_001369716.1:p.Phe1212Val
NM_001382788.1:c.3589T>G	NP_001369717.1:p.Phe1197Val
NM_001382789.1:c.3580T>G	NP_001369718.1:p.Phe1194Val
NM_001382790.1:c.3556T>G	NP_001369719.1:p.Phe1186Val
NM_001382791.1:c.3550T>G	NP_001369720.1:p.Phe1184Val
NM_001382792.1:c.3523T>G	NP_001369721.1:p.Phe1175Val
NM_001382793.1:c.3517T>G	NP_001369722.1:p.Phe1173Val
NM_001382794.1:c.3517T>G	NP_001369723.1:p.Phe1173Val
NM_001382795.1:c.3511T>G	NP_001369724.1:p.Phe1171Val
NM_001382796.1:c.3472T>G	NP_001369725.1:p.Phe1158Val
NM_001382797.1:c.3460T>G	NP_001369726.1:p.Phe1154Val
NM_001382798.1:c.3403T>G	NP_001369727.1:p.Phe1135Val
NM_001382799.1:c.3379T>G	NP_001369728.1:p.Phe1127Val
NM_001382800.1:c.3373T>G	NP_001369729.1:p.Phe1125Val
NM_001382801.1:c.3355T>G	NP_001369730.1:p.Phe1119Val
NM_001382802.1:c.3301T>G	NP_001369731.1:p.Phe1101Val
NM_001382803.1:c.*138T>G	NP_001369732.1:n.*138T>G
NM_001382804.1:c.2731T>G	NP_001369733.1:p.Phe911Val
NM_001382805.1:c.2608T>G	NP_001369734.1:p.Phe870Val
NM_001382806.1:c.2521T>G	NP_001369735.1:p.Phe841Val
NM_004448.4:c.3559T>G MANE Select	NP_004439.2:p.Phe1187Val
NR_110535.2:n.3797T>G