Canonical Allele Identifier: CA399313040

Gene: ERBB2

Linked Data

• dbSNP Id: rs150680317
• MyVariant Identifiers: chr17:g.37884011G>C (hg19) ; chr17:g.39727758G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727758G>C , CM000679.2:g.39727758G>C	GRCh38
NC_000017.10:g.37884011G>C , CM000679.1:g.37884011G>C	GRCh37
NC_000017.9:g.35137537G>C	NCBI36
NG_007503.1:g.44619G>C , LRG_724:g.44619G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3482G>C MANE Select	ENSP00000269571.4:p.Arg1161Pro
ENST00000269571.9:c.3482G>C	ENSP00000269571.4:p.Arg1161Pro
ENST00000406381.6:c.3392G>C	ENSP00000385185.2:p.Arg1131Pro
ENST00000445658.6:c.2654G>C	ENSP00000404047.2:p.Arg885Pro
ENST00000541774.5:c.3437G>C	ENSP00000446466.1:p.Arg1146Pro
ENST00000578373.5:c.*3272G>C	ENSP00000463427.1:n.*3272G>C
ENST00000584450.5:c.*61G>C	ENSP00000463714.1:n.*61G>C
ENST00000584601.5:c.3392G>C	ENSP00000462438.1:p.Arg1131Pro
NM_001005862.2:c.3392G>C , LRG_724t1:c.3392G>C	NP_001005862.1:p.Arg1131Pro
NM_001289936.1:c.3437G>C , LRG_724t4:c.3437G>C	NP_001276865.1:p.Arg1146Pro
NM_001289937.1:c.*61G>C	NP_001276866.1:n.*61G>C
NM_004448.3:c.3482G>C , LRG_724t2:c.3482G>C	NP_004439.2:p.Arg1161Pro
NR_110535.1:n.3806G>C
XM_024450641.1:c.3620G>C	XP_024306409.1:p.Arg1207Pro
XM_024450642.1:c.3575G>C	XP_024306410.1:p.Arg1192Pro
XM_024450643.1:c.3530G>C	XP_024306411.1:p.Arg1177Pro
NM_001005862.3:c.3392G>C	NP_001005862.1:p.Arg1131Pro
NM_001289936.2:c.3437G>C	NP_001276865.1:p.Arg1146Pro
NM_001289937.2:c.*61G>C	NP_001276866.1:n.*61G>C
NM_001382782.1:c.3392G>C	NP_001369711.1:p.Arg1131Pro
NM_001382783.1:c.3392G>C	NP_001369712.1:p.Arg1131Pro
NM_001382784.1:c.3599G>C	NP_001369713.1:p.Arg1200Pro
NM_001382785.1:c.3584G>C	NP_001369714.1:p.Arg1195Pro
NM_001382786.1:c.3563G>C	NP_001369715.1:p.Arg1188Pro
NM_001382787.1:c.3557G>C	NP_001369716.1:p.Arg1186Pro
NM_001382788.1:c.3512G>C	NP_001369717.1:p.Arg1171Pro
NM_001382789.1:c.3503G>C	NP_001369718.1:p.Arg1168Pro
NM_001382790.1:c.3479G>C	NP_001369719.1:p.Arg1160Pro
NM_001382791.1:c.3473G>C	NP_001369720.1:p.Arg1158Pro
NM_001382792.1:c.3446G>C	NP_001369721.1:p.Arg1149Pro
NM_001382793.1:c.3440G>C	NP_001369722.1:p.Arg1147Pro
NM_001382794.1:c.3440G>C	NP_001369723.1:p.Arg1147Pro
NM_001382795.1:c.3434G>C	NP_001369724.1:p.Arg1145Pro
NM_001382796.1:c.3395G>C	NP_001369725.1:p.Arg1132Pro
NM_001382797.1:c.3383G>C	NP_001369726.1:p.Arg1128Pro
NM_001382798.1:c.3326G>C	NP_001369727.1:p.Arg1109Pro
NM_001382799.1:c.3302G>C	NP_001369728.1:p.Arg1101Pro
NM_001382800.1:c.3296G>C	NP_001369729.1:p.Arg1099Pro
NM_001382801.1:c.3278G>C	NP_001369730.1:p.Arg1093Pro
NM_001382802.1:c.3224G>C	NP_001369731.1:p.Arg1075Pro
NM_001382803.1:c.*61G>C	NP_001369732.1:n.*61G>C
NM_001382804.1:c.2654G>C	NP_001369733.1:p.Arg885Pro
NM_001382805.1:c.2531G>C	NP_001369734.1:p.Arg844Pro
NM_001382806.1:c.2444G>C	NP_001369735.1:p.Arg815Pro
NM_004448.4:c.3482G>C MANE Select	NP_004439.2:p.Arg1161Pro
NR_110535.2:n.3720G>C