Canonical Allele Identifier: CA399310797

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143247688
• MyVariant Identifiers: chr17:g.37883683C>G (hg19) ; chr17:g.39727430C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727430C>G , CM000679.2:g.39727430C>G	GRCh38
NC_000017.10:g.37883683C>G , CM000679.1:g.37883683C>G	GRCh37
NC_000017.9:g.35137209C>G	NCBI36
NG_007503.1:g.44291C>G , LRG_724:g.44291C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3295C>G MANE Select	ENSP00000269571.4:p.Gln1099Glu
ENST00000269571.9:c.3295C>G	ENSP00000269571.4:p.Gln1099Glu
ENST00000406381.6:c.3205C>G	ENSP00000385185.2:p.Gln1069Glu
ENST00000445658.6:c.2467C>G	ENSP00000404047.2:p.Gln823Glu
ENST00000541774.5:c.3250C>G	ENSP00000446466.1:p.Gln1084Glu
ENST00000578373.5:c.*3085C>G	ENSP00000463427.1:n.*3085C>G
ENST00000584450.5:c.3160-259C>G	ENSP00000463714.1:n.3160-259C>G
ENST00000584601.5:c.3205C>G	ENSP00000462438.1:p.Gln1069Glu
NM_001005862.2:c.3205C>G , LRG_724t1:c.3205C>G	NP_001005862.1:p.Gln1069Glu
NM_001289936.1:c.3250C>G , LRG_724t4:c.3250C>G	NP_001276865.1:p.Gln1084Glu
NM_001289937.1:c.3160-259C>G	NP_001276866.1:n.3160-259C>G
NM_004448.3:c.3295C>G , LRG_724t2:c.3295C>G	NP_004439.2:p.Gln1099Glu
NR_110535.1:n.3619C>G
XM_024450641.1:c.3433C>G	XP_024306409.1:p.Gln1145Glu
XM_024450642.1:c.3388C>G	XP_024306410.1:p.Gln1130Glu
XM_024450643.1:c.3343C>G	XP_024306411.1:p.Gln1115Glu
NM_001005862.3:c.3205C>G	NP_001005862.1:p.Gln1069Glu
NM_001289936.2:c.3250C>G	NP_001276865.1:p.Gln1084Glu
NM_001289937.2:c.3160-259C>G	NP_001276866.1:n.3160-259C>G
NM_001382782.1:c.3205C>G	NP_001369711.1:p.Gln1069Glu
NM_001382783.1:c.3205C>G	NP_001369712.1:p.Gln1069Glu
NM_001382784.1:c.3412C>G	NP_001369713.1:p.Gln1138Glu
NM_001382785.1:c.3397C>G	NP_001369714.1:p.Gln1133Glu
NM_001382786.1:c.3376C>G	NP_001369715.1:p.Gln1126Glu
NM_001382787.1:c.3370C>G	NP_001369716.1:p.Gln1124Glu
NM_001382788.1:c.3325C>G	NP_001369717.1:p.Gln1109Glu
NM_001382789.1:c.3316C>G	NP_001369718.1:p.Gln1106Glu
NM_001382790.1:c.3292C>G	NP_001369719.1:p.Gln1098Glu
NM_001382791.1:c.3286C>G	NP_001369720.1:p.Gln1096Glu
NM_001382792.1:c.3259C>G	NP_001369721.1:p.Gln1087Glu
NM_001382793.1:c.3253C>G	NP_001369722.1:p.Gln1085Glu
NM_001382794.1:c.3253C>G	NP_001369723.1:p.Gln1085Glu
NM_001382795.1:c.3247C>G	NP_001369724.1:p.Gln1083Glu
NM_001382796.1:c.3208C>G	NP_001369725.1:p.Gln1070Glu
NM_001382797.1:c.3196C>G	NP_001369726.1:p.Gln1066Glu
NM_001382798.1:c.3139C>G	NP_001369727.1:p.Gln1047Glu
NM_001382799.1:c.3115C>G	NP_001369728.1:p.Gln1039Glu
NM_001382800.1:c.3109C>G	NP_001369729.1:p.Gln1037Glu
NM_001382801.1:c.3091C>G	NP_001369730.1:p.Gln1031Glu
NM_001382802.1:c.3037C>G	NP_001369731.1:p.Gln1013Glu
NM_001382803.1:c.3118-259C>G	NP_001369732.1:n.3118-259C>G
NM_001382804.1:c.2467C>G	NP_001369733.1:p.Gln823Glu
NM_001382805.1:c.2344C>G	NP_001369734.1:p.Gln782Glu
NM_001382806.1:c.2257C>G	NP_001369735.1:p.Gln753Glu
NM_004448.4:c.3295C>G MANE Select	NP_004439.2:p.Gln1099Glu
NR_110535.2:n.3533C>G