Canonical Allele Identifier: CA399313770

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37884113A>C (hg19) ; chr17:g.39727860A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727860A>C , CM000679.2:g.39727860A>C	GRCh38
NC_000017.10:g.37884113A>C , CM000679.1:g.37884113A>C	GRCh37
NC_000017.9:g.35137639A>C	NCBI36
NG_007503.1:g.44721A>C , LRG_724:g.44721A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3584A>C MANE Select	ENSP00000269571.4:p.Glu1195Ala
ENST00000269571.9:c.3584A>C	ENSP00000269571.4:p.Glu1195Ala
ENST00000406381.6:c.3494A>C	ENSP00000385185.2:p.Glu1165Ala
ENST00000445658.6:c.2756A>C	ENSP00000404047.2:p.Glu919Ala
ENST00000541774.5:c.3539A>C	ENSP00000446466.1:p.Glu1180Ala
ENST00000578373.5:c.*3374A>C	ENSP00000463427.1:n.*3374A>C
ENST00000584450.5:c.*163A>C	ENSP00000463714.1:n.*163A>C
ENST00000584601.5:c.3494A>C	ENSP00000462438.1:p.Glu1165Ala
NM_001005862.2:c.3494A>C , LRG_724t1:c.3494A>C	NP_001005862.1:p.Glu1165Ala
NM_001289936.1:c.3539A>C , LRG_724t4:c.3539A>C	NP_001276865.1:p.Glu1180Ala
NM_001289937.1:c.*163A>C	NP_001276866.1:n.*163A>C
NM_004448.3:c.3584A>C , LRG_724t2:c.3584A>C	NP_004439.2:p.Glu1195Ala
NR_110535.1:n.3908A>C
XM_024450641.1:c.3722A>C	XP_024306409.1:p.Glu1241Ala
XM_024450642.1:c.3677A>C	XP_024306410.1:p.Glu1226Ala
XM_024450643.1:c.3632A>C	XP_024306411.1:p.Glu1211Ala
NM_001005862.3:c.3494A>C	NP_001005862.1:p.Glu1165Ala
NM_001289936.2:c.3539A>C	NP_001276865.1:p.Glu1180Ala
NM_001289937.2:c.*163A>C	NP_001276866.1:n.*163A>C
NM_001382782.1:c.3494A>C	NP_001369711.1:p.Glu1165Ala
NM_001382783.1:c.3494A>C	NP_001369712.1:p.Glu1165Ala
NM_001382784.1:c.3701A>C	NP_001369713.1:p.Glu1234Ala
NM_001382785.1:c.3686A>C	NP_001369714.1:p.Glu1229Ala
NM_001382786.1:c.3665A>C	NP_001369715.1:p.Glu1222Ala
NM_001382787.1:c.3659A>C	NP_001369716.1:p.Glu1220Ala
NM_001382788.1:c.3614A>C	NP_001369717.1:p.Glu1205Ala
NM_001382789.1:c.3605A>C	NP_001369718.1:p.Glu1202Ala
NM_001382790.1:c.3581A>C	NP_001369719.1:p.Glu1194Ala
NM_001382791.1:c.3575A>C	NP_001369720.1:p.Glu1192Ala
NM_001382792.1:c.3548A>C	NP_001369721.1:p.Glu1183Ala
NM_001382793.1:c.3542A>C	NP_001369722.1:p.Glu1181Ala
NM_001382794.1:c.3542A>C	NP_001369723.1:p.Glu1181Ala
NM_001382795.1:c.3536A>C	NP_001369724.1:p.Glu1179Ala
NM_001382796.1:c.3497A>C	NP_001369725.1:p.Glu1166Ala
NM_001382797.1:c.3485A>C	NP_001369726.1:p.Glu1162Ala
NM_001382798.1:c.3428A>C	NP_001369727.1:p.Glu1143Ala
NM_001382799.1:c.3404A>C	NP_001369728.1:p.Glu1135Ala
NM_001382800.1:c.3398A>C	NP_001369729.1:p.Glu1133Ala
NM_001382801.1:c.3380A>C	NP_001369730.1:p.Glu1127Ala
NM_001382802.1:c.3326A>C	NP_001369731.1:p.Glu1109Ala
NM_001382803.1:c.*163A>C	NP_001369732.1:n.*163A>C
NM_001382804.1:c.2756A>C	NP_001369733.1:p.Glu919Ala
NM_001382805.1:c.2633A>C	NP_001369734.1:p.Glu878Ala
NM_001382806.1:c.2546A>C	NP_001369735.1:p.Glu849Ala
NM_004448.4:c.3584A>C MANE Select	NP_004439.2:p.Glu1195Ala
NR_110535.2:n.3822A>C