Canonical Allele Identifier: CA399313570

Gene: ERBB2

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3559T>C MANE Select	ENSP00000269571.4:p.Phe1187Leu
ENST00000269571.9:c.3559T>C	ENSP00000269571.4:p.Phe1187Leu
ENST00000406381.6:c.3469T>C	ENSP00000385185.2:p.Phe1157Leu
ENST00000445658.6:c.2731T>C	ENSP00000404047.2:p.Phe911Leu
ENST00000541774.5:c.3514T>C	ENSP00000446466.1:p.Phe1172Leu
ENST00000578373.5:c.*3349T>C	ENSP00000463427.1:n.*3349T>C
ENST00000584450.5:c.*138T>C	ENSP00000463714.1:n.*138T>C
ENST00000584601.5:c.3469T>C	ENSP00000462438.1:p.Phe1157Leu
NM_001005862.2:c.3469T>C , LRG_724t1:c.3469T>C	NP_001005862.1:p.Phe1157Leu
NM_001289936.1:c.3514T>C , LRG_724t4:c.3514T>C	NP_001276865.1:p.Phe1172Leu
NM_001289937.1:c.*138T>C	NP_001276866.1:n.*138T>C
NM_004448.3:c.3559T>C , LRG_724t2:c.3559T>C	NP_004439.2:p.Phe1187Leu
NR_110535.1:n.3883T>C
XM_024450641.1:c.3697T>C	XP_024306409.1:p.Phe1233Leu
XM_024450642.1:c.3652T>C	XP_024306410.1:p.Phe1218Leu
XM_024450643.1:c.3607T>C	XP_024306411.1:p.Phe1203Leu
NM_001005862.3:c.3469T>C	NP_001005862.1:p.Phe1157Leu
NM_001289936.2:c.3514T>C	NP_001276865.1:p.Phe1172Leu
NM_001289937.2:c.*138T>C	NP_001276866.1:n.*138T>C
NM_001382782.1:c.3469T>C	NP_001369711.1:p.Phe1157Leu
NM_001382783.1:c.3469T>C	NP_001369712.1:p.Phe1157Leu
NM_001382784.1:c.3676T>C	NP_001369713.1:p.Phe1226Leu
NM_001382785.1:c.3661T>C	NP_001369714.1:p.Phe1221Leu
NM_001382786.1:c.3640T>C	NP_001369715.1:p.Phe1214Leu
NM_001382787.1:c.3634T>C	NP_001369716.1:p.Phe1212Leu
NM_001382788.1:c.3589T>C	NP_001369717.1:p.Phe1197Leu
NM_001382789.1:c.3580T>C	NP_001369718.1:p.Phe1194Leu
NM_001382790.1:c.3556T>C	NP_001369719.1:p.Phe1186Leu
NM_001382791.1:c.3550T>C	NP_001369720.1:p.Phe1184Leu
NM_001382792.1:c.3523T>C	NP_001369721.1:p.Phe1175Leu
NM_001382793.1:c.3517T>C	NP_001369722.1:p.Phe1173Leu
NM_001382794.1:c.3517T>C	NP_001369723.1:p.Phe1173Leu
NM_001382795.1:c.3511T>C	NP_001369724.1:p.Phe1171Leu
NM_001382796.1:c.3472T>C	NP_001369725.1:p.Phe1158Leu
NM_001382797.1:c.3460T>C	NP_001369726.1:p.Phe1154Leu
NM_001382798.1:c.3403T>C	NP_001369727.1:p.Phe1135Leu
NM_001382799.1:c.3379T>C	NP_001369728.1:p.Phe1127Leu
NM_001382800.1:c.3373T>C	NP_001369729.1:p.Phe1125Leu
NM_001382801.1:c.3355T>C	NP_001369730.1:p.Phe1119Leu
NM_001382802.1:c.3301T>C	NP_001369731.1:p.Phe1101Leu
NM_001382803.1:c.*138T>C	NP_001369732.1:n.*138T>C
NM_001382804.1:c.2731T>C	NP_001369733.1:p.Phe911Leu
NM_001382805.1:c.2608T>C	NP_001369734.1:p.Phe870Leu
NM_001382806.1:c.2521T>C	NP_001369735.1:p.Phe841Leu
NM_004448.4:c.3559T>C MANE Select	NP_004439.2:p.Phe1187Leu
NR_110535.2:n.3797T>C