Canonical Allele Identifier: CA399310246

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37883589A>C (hg19) ; chr17:g.39727336A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727336A>C , CM000679.2:g.39727336A>C	GRCh38
NC_000017.10:g.37883589A>C , CM000679.1:g.37883589A>C	GRCh37
NC_000017.9:g.35137115A>C	NCBI36
NG_007503.1:g.44197A>C , LRG_724:g.44197A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3201A>C MANE Select	ENSP00000269571.4:p.Glu1067Asp
ENST00000269571.9:c.3201A>C	ENSP00000269571.4:p.Glu1067Asp
ENST00000406381.6:c.3111A>C	ENSP00000385185.2:p.Glu1037Asp
ENST00000445658.6:c.2373A>C	ENSP00000404047.2:p.Glu791Asp
ENST00000541774.5:c.3156A>C	ENSP00000446466.1:p.Glu1052Asp
ENST00000578373.5:c.*2991A>C	ENSP00000463427.1:n.*2991A>C
ENST00000584450.5:c.3159+333A>C	ENSP00000463714.1:n.3159+333A>C
ENST00000584601.5:c.3111A>C	ENSP00000462438.1:p.Glu1037Asp
NM_001005862.2:c.3111A>C , LRG_724t1:c.3111A>C	NP_001005862.1:p.Glu1037Asp
NM_001289936.1:c.3156A>C , LRG_724t4:c.3156A>C	NP_001276865.1:p.Glu1052Asp
NM_001289937.1:c.3159+333A>C	NP_001276866.1:n.3159+333A>C
NM_004448.3:c.3201A>C , LRG_724t2:c.3201A>C	NP_004439.2:p.Glu1067Asp
NR_110535.1:n.3525A>C
XM_024450641.1:c.3339A>C	XP_024306409.1:p.Glu1113Asp
XM_024450642.1:c.3294A>C	XP_024306410.1:p.Glu1098Asp
XM_024450643.1:c.3249A>C	XP_024306411.1:p.Glu1083Asp
NM_001005862.3:c.3111A>C	NP_001005862.1:p.Glu1037Asp
NM_001289936.2:c.3156A>C	NP_001276865.1:p.Glu1052Asp
NM_001289937.2:c.3159+333A>C	NP_001276866.1:n.3159+333A>C
NM_001382782.1:c.3111A>C	NP_001369711.1:p.Glu1037Asp
NM_001382783.1:c.3111A>C	NP_001369712.1:p.Glu1037Asp
NM_001382784.1:c.3318A>C	NP_001369713.1:p.Glu1106Asp
NM_001382785.1:c.3303A>C	NP_001369714.1:p.Glu1101Asp
NM_001382786.1:c.3282A>C	NP_001369715.1:p.Glu1094Asp
NM_001382787.1:c.3276A>C	NP_001369716.1:p.Glu1092Asp
NM_001382788.1:c.3231A>C	NP_001369717.1:p.Glu1077Asp
NM_001382789.1:c.3222A>C	NP_001369718.1:p.Glu1074Asp
NM_001382790.1:c.3198A>C	NP_001369719.1:p.Glu1066Asp
NM_001382791.1:c.3192A>C	NP_001369720.1:p.Glu1064Asp
NM_001382792.1:c.3165A>C	NP_001369721.1:p.Glu1055Asp
NM_001382793.1:c.3159A>C	NP_001369722.1:p.Glu1053Asp
NM_001382794.1:c.3159A>C	NP_001369723.1:p.Glu1053Asp
NM_001382795.1:c.3153A>C	NP_001369724.1:p.Glu1051Asp
NM_001382796.1:c.3114A>C	NP_001369725.1:p.Glu1038Asp
NM_001382797.1:c.3102A>C	NP_001369726.1:p.Glu1034Asp
NM_001382798.1:c.3045A>C	NP_001369727.1:p.Glu1015Asp
NM_001382799.1:c.3021A>C	NP_001369728.1:p.Glu1007Asp
NM_001382800.1:c.3015A>C	NP_001369729.1:p.Glu1005Asp
NM_001382801.1:c.2997A>C	NP_001369730.1:p.Glu999Asp
NM_001382802.1:c.2943A>C	NP_001369731.1:p.Glu981Asp
NM_001382803.1:c.3117+333A>C	NP_001369732.1:n.3117+333A>C
NM_001382804.1:c.2373A>C	NP_001369733.1:p.Glu791Asp
NM_001382805.1:c.2250A>C	NP_001369734.1:p.Glu750Asp
NM_001382806.1:c.2163A>C	NP_001369735.1:p.Glu721Asp
NM_004448.4:c.3201A>C MANE Select	NP_004439.2:p.Glu1067Asp
NR_110535.2:n.3439A>C