Canonical Allele Identifier: CA399314200

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143311085
• MyVariant Identifiers: chr17:g.37884171C>A (hg19) ; chr17:g.39727918C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727918C>A , CM000679.2:g.39727918C>A	GRCh38
NC_000017.10:g.37884171C>A , CM000679.1:g.37884171C>A	GRCh37
NC_000017.9:g.35137697C>A	NCBI36
NG_007503.1:g.44779C>A , LRG_724:g.44779C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3642C>A MANE Select	ENSP00000269571.4:p.Ser1214Arg
ENST00000269571.9:c.3642C>A	ENSP00000269571.4:p.Ser1214Arg
ENST00000406381.6:c.3552C>A	ENSP00000385185.2:p.Ser1184Arg
ENST00000445658.6:c.2814C>A	ENSP00000404047.2:p.Ser938Arg
ENST00000541774.5:c.3597C>A	ENSP00000446466.1:p.Ser1199Arg
ENST00000578373.5:c.*3432C>A	ENSP00000463427.1:n.*3432C>A
ENST00000584450.5:c.*221C>A	ENSP00000463714.1:n.*221C>A
ENST00000584601.5:c.3552C>A	ENSP00000462438.1:p.Ser1184Arg
NM_001005862.2:c.3552C>A , LRG_724t1:c.3552C>A	NP_001005862.1:p.Ser1184Arg
NM_001289936.1:c.3597C>A , LRG_724t4:c.3597C>A	NP_001276865.1:p.Ser1199Arg
NM_001289937.1:c.*221C>A	NP_001276866.1:n.*221C>A
NM_004448.3:c.3642C>A , LRG_724t2:c.3642C>A	NP_004439.2:p.Ser1214Arg
NR_110535.1:n.3966C>A
XM_024450641.1:c.3780C>A	XP_024306409.1:p.Ser1260Arg
XM_024450642.1:c.3735C>A	XP_024306410.1:p.Ser1245Arg
XM_024450643.1:c.3690C>A	XP_024306411.1:p.Ser1230Arg
NM_001005862.3:c.3552C>A	NP_001005862.1:p.Ser1184Arg
NM_001289936.2:c.3597C>A	NP_001276865.1:p.Ser1199Arg
NM_001289937.2:c.*221C>A	NP_001276866.1:n.*221C>A
NM_001382782.1:c.3552C>A	NP_001369711.1:p.Ser1184Arg
NM_001382783.1:c.3552C>A	NP_001369712.1:p.Ser1184Arg
NM_001382784.1:c.3759C>A	NP_001369713.1:p.Ser1253Arg
NM_001382785.1:c.3744C>A	NP_001369714.1:p.Ser1248Arg
NM_001382786.1:c.3723C>A	NP_001369715.1:p.Ser1241Arg
NM_001382787.1:c.3717C>A	NP_001369716.1:p.Ser1239Arg
NM_001382788.1:c.3672C>A	NP_001369717.1:p.Ser1224Arg
NM_001382789.1:c.3663C>A	NP_001369718.1:p.Ser1221Arg
NM_001382790.1:c.3639C>A	NP_001369719.1:p.Ser1213Arg
NM_001382791.1:c.3633C>A	NP_001369720.1:p.Ser1211Arg
NM_001382792.1:c.3606C>A	NP_001369721.1:p.Ser1202Arg
NM_001382793.1:c.3600C>A	NP_001369722.1:p.Ser1200Arg
NM_001382794.1:c.3600C>A	NP_001369723.1:p.Ser1200Arg
NM_001382795.1:c.3594C>A	NP_001369724.1:p.Ser1198Arg
NM_001382796.1:c.3555C>A	NP_001369725.1:p.Ser1185Arg
NM_001382797.1:c.3543C>A	NP_001369726.1:p.Ser1181Arg
NM_001382798.1:c.3486C>A	NP_001369727.1:p.Ser1162Arg
NM_001382799.1:c.3462C>A	NP_001369728.1:p.Ser1154Arg
NM_001382800.1:c.3456C>A	NP_001369729.1:p.Ser1152Arg
NM_001382801.1:c.3438C>A	NP_001369730.1:p.Ser1146Arg
NM_001382802.1:c.3384C>A	NP_001369731.1:p.Ser1128Arg
NM_001382803.1:c.*221C>A	NP_001369732.1:n.*221C>A
NM_001382804.1:c.2814C>A	NP_001369733.1:p.Ser938Arg
NM_001382805.1:c.2691C>A	NP_001369734.1:p.Ser897Arg
NM_001382806.1:c.2604C>A	NP_001369735.1:p.Ser868Arg
NM_004448.4:c.3642C>A MANE Select	NP_004439.2:p.Ser1214Arg
NR_110535.2:n.3880C>A