Canonical Allele Identifier: CA399313142

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143295461
• MyVariant Identifiers: chr17:g.37884028C>G (hg19) ; chr17:g.39727775C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727775C>G , CM000679.2:g.39727775C>G	GRCh38
NC_000017.10:g.37884028C>G , CM000679.1:g.37884028C>G	GRCh37
NC_000017.9:g.35137554C>G	NCBI36
NG_007503.1:g.44636C>G , LRG_724:g.44636C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3499C>G MANE Select	ENSP00000269571.4:p.Leu1167Val
ENST00000269571.9:c.3499C>G	ENSP00000269571.4:p.Leu1167Val
ENST00000406381.6:c.3409C>G	ENSP00000385185.2:p.Leu1137Val
ENST00000445658.6:c.2671C>G	ENSP00000404047.2:p.Leu891Val
ENST00000541774.5:c.3454C>G	ENSP00000446466.1:p.Leu1152Val
ENST00000578373.5:c.*3289C>G	ENSP00000463427.1:n.*3289C>G
ENST00000584450.5:c.*78C>G	ENSP00000463714.1:n.*78C>G
ENST00000584601.5:c.3409C>G	ENSP00000462438.1:p.Leu1137Val
NM_001005862.2:c.3409C>G , LRG_724t1:c.3409C>G	NP_001005862.1:p.Leu1137Val
NM_001289936.1:c.3454C>G , LRG_724t4:c.3454C>G	NP_001276865.1:p.Leu1152Val
NM_001289937.1:c.*78C>G	NP_001276866.1:n.*78C>G
NM_004448.3:c.3499C>G , LRG_724t2:c.3499C>G	NP_004439.2:p.Leu1167Val
NR_110535.1:n.3823C>G
XM_024450641.1:c.3637C>G	XP_024306409.1:p.Leu1213Val
XM_024450642.1:c.3592C>G	XP_024306410.1:p.Leu1198Val
XM_024450643.1:c.3547C>G	XP_024306411.1:p.Leu1183Val
NM_001005862.3:c.3409C>G	NP_001005862.1:p.Leu1137Val
NM_001289936.2:c.3454C>G	NP_001276865.1:p.Leu1152Val
NM_001289937.2:c.*78C>G	NP_001276866.1:n.*78C>G
NM_001382782.1:c.3409C>G	NP_001369711.1:p.Leu1137Val
NM_001382783.1:c.3409C>G	NP_001369712.1:p.Leu1137Val
NM_001382784.1:c.3616C>G	NP_001369713.1:p.Leu1206Val
NM_001382785.1:c.3601C>G	NP_001369714.1:p.Leu1201Val
NM_001382786.1:c.3580C>G	NP_001369715.1:p.Leu1194Val
NM_001382787.1:c.3574C>G	NP_001369716.1:p.Leu1192Val
NM_001382788.1:c.3529C>G	NP_001369717.1:p.Leu1177Val
NM_001382789.1:c.3520C>G	NP_001369718.1:p.Leu1174Val
NM_001382790.1:c.3496C>G	NP_001369719.1:p.Leu1166Val
NM_001382791.1:c.3490C>G	NP_001369720.1:p.Leu1164Val
NM_001382792.1:c.3463C>G	NP_001369721.1:p.Leu1155Val
NM_001382793.1:c.3457C>G	NP_001369722.1:p.Leu1153Val
NM_001382794.1:c.3457C>G	NP_001369723.1:p.Leu1153Val
NM_001382795.1:c.3451C>G	NP_001369724.1:p.Leu1151Val
NM_001382796.1:c.3412C>G	NP_001369725.1:p.Leu1138Val
NM_001382797.1:c.3400C>G	NP_001369726.1:p.Leu1134Val
NM_001382798.1:c.3343C>G	NP_001369727.1:p.Leu1115Val
NM_001382799.1:c.3319C>G	NP_001369728.1:p.Leu1107Val
NM_001382800.1:c.3313C>G	NP_001369729.1:p.Leu1105Val
NM_001382801.1:c.3295C>G	NP_001369730.1:p.Leu1099Val
NM_001382802.1:c.3241C>G	NP_001369731.1:p.Leu1081Val
NM_001382803.1:c.*78C>G	NP_001369732.1:n.*78C>G
NM_001382804.1:c.2671C>G	NP_001369733.1:p.Leu891Val
NM_001382805.1:c.2548C>G	NP_001369734.1:p.Leu850Val
NM_001382806.1:c.2461C>G	NP_001369735.1:p.Leu821Val
NM_004448.4:c.3499C>G MANE Select	NP_004439.2:p.Leu1167Val
NR_110535.2:n.3737C>G