Canonical Allele Identifier: CA399313096

Gene: ERBB2

Linked Data

• dbSNP Id: rs1248880121
• MyVariant Identifiers: chr17:g.37884020G>C (hg19) ; chr17:g.39727767G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727767G>C , CM000679.2:g.39727767G>C	GRCh38
NC_000017.10:g.37884020G>C , CM000679.1:g.37884020G>C	GRCh37
NC_000017.9:g.35137546G>C	NCBI36
NG_007503.1:g.44628G>C , LRG_724:g.44628G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3491G>C MANE Select	ENSP00000269571.4:p.Gly1164Ala
ENST00000269571.9:c.3491G>C	ENSP00000269571.4:p.Gly1164Ala
ENST00000406381.6:c.3401G>C	ENSP00000385185.2:p.Gly1134Ala
ENST00000445658.6:c.2663G>C	ENSP00000404047.2:p.Gly888Ala
ENST00000541774.5:c.3446G>C	ENSP00000446466.1:p.Gly1149Ala
ENST00000578373.5:c.*3281G>C	ENSP00000463427.1:n.*3281G>C
ENST00000584450.5:c.*70G>C	ENSP00000463714.1:n.*70G>C
ENST00000584601.5:c.3401G>C	ENSP00000462438.1:p.Gly1134Ala
NM_001005862.2:c.3401G>C , LRG_724t1:c.3401G>C	NP_001005862.1:p.Gly1134Ala
NM_001289936.1:c.3446G>C , LRG_724t4:c.3446G>C	NP_001276865.1:p.Gly1149Ala
NM_001289937.1:c.*70G>C	NP_001276866.1:n.*70G>C
NM_004448.3:c.3491G>C , LRG_724t2:c.3491G>C	NP_004439.2:p.Gly1164Ala
NR_110535.1:n.3815G>C
XM_024450641.1:c.3629G>C	XP_024306409.1:p.Gly1210Ala
XM_024450642.1:c.3584G>C	XP_024306410.1:p.Gly1195Ala
XM_024450643.1:c.3539G>C	XP_024306411.1:p.Gly1180Ala
NM_001005862.3:c.3401G>C	NP_001005862.1:p.Gly1134Ala
NM_001289936.2:c.3446G>C	NP_001276865.1:p.Gly1149Ala
NM_001289937.2:c.*70G>C	NP_001276866.1:n.*70G>C
NM_001382782.1:c.3401G>C	NP_001369711.1:p.Gly1134Ala
NM_001382783.1:c.3401G>C	NP_001369712.1:p.Gly1134Ala
NM_001382784.1:c.3608G>C	NP_001369713.1:p.Gly1203Ala
NM_001382785.1:c.3593G>C	NP_001369714.1:p.Gly1198Ala
NM_001382786.1:c.3572G>C	NP_001369715.1:p.Gly1191Ala
NM_001382787.1:c.3566G>C	NP_001369716.1:p.Gly1189Ala
NM_001382788.1:c.3521G>C	NP_001369717.1:p.Gly1174Ala
NM_001382789.1:c.3512G>C	NP_001369718.1:p.Gly1171Ala
NM_001382790.1:c.3488G>C	NP_001369719.1:p.Gly1163Ala
NM_001382791.1:c.3482G>C	NP_001369720.1:p.Gly1161Ala
NM_001382792.1:c.3455G>C	NP_001369721.1:p.Gly1152Ala
NM_001382793.1:c.3449G>C	NP_001369722.1:p.Gly1150Ala
NM_001382794.1:c.3449G>C	NP_001369723.1:p.Gly1150Ala
NM_001382795.1:c.3443G>C	NP_001369724.1:p.Gly1148Ala
NM_001382796.1:c.3404G>C	NP_001369725.1:p.Gly1135Ala
NM_001382797.1:c.3392G>C	NP_001369726.1:p.Gly1131Ala
NM_001382798.1:c.3335G>C	NP_001369727.1:p.Gly1112Ala
NM_001382799.1:c.3311G>C	NP_001369728.1:p.Gly1104Ala
NM_001382800.1:c.3305G>C	NP_001369729.1:p.Gly1102Ala
NM_001382801.1:c.3287G>C	NP_001369730.1:p.Gly1096Ala
NM_001382802.1:c.3233G>C	NP_001369731.1:p.Gly1078Ala
NM_001382803.1:c.*70G>C	NP_001369732.1:n.*70G>C
NM_001382804.1:c.2663G>C	NP_001369733.1:p.Gly888Ala
NM_001382805.1:c.2540G>C	NP_001369734.1:p.Gly847Ala
NM_001382806.1:c.2453G>C	NP_001369735.1:p.Gly818Ala
NM_004448.4:c.3491G>C MANE Select	NP_004439.2:p.Gly1164Ala
NR_110535.2:n.3729G>C