Canonical Allele Identifier: CA399312805

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143261917
• MyVariant Identifiers: chr17:g.37883800G>T (hg19) ; chr17:g.39727547G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727547G>T , CM000679.2:g.39727547G>T	GRCh38
NC_000017.10:g.37883800G>T , CM000679.1:g.37883800G>T	GRCh37
NC_000017.9:g.35137326G>T	NCBI36
NG_007503.1:g.44408G>T , LRG_724:g.44408G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3412G>T MANE Select	ENSP00000269571.4:p.Glu1138Ter
ENST00000269571.9:c.3412G>T	ENSP00000269571.4:p.Glu1138Ter
ENST00000406381.6:c.3322G>T	ENSP00000385185.2:p.Glu1108Ter
ENST00000445658.6:c.2584G>T	ENSP00000404047.2:p.Glu862Ter
ENST00000541774.5:c.3367G>T	ENSP00000446466.1:p.Glu1123Ter
ENST00000578373.5:c.*3202G>T	ENSP00000463427.1:n.*3202G>T
ENST00000584450.5:c.3160-142G>T	ENSP00000463714.1:n.3160-142G>T
ENST00000584601.5:c.3322G>T	ENSP00000462438.1:p.Glu1108Ter
NM_001005862.2:c.3322G>T , LRG_724t1:c.3322G>T	NP_001005862.1:p.Glu1108Ter
NM_001289936.1:c.3367G>T , LRG_724t4:c.3367G>T	NP_001276865.1:p.Glu1123Ter
NM_001289937.1:c.3160-142G>T	NP_001276866.1:n.3160-142G>T
NM_004448.3:c.3412G>T , LRG_724t2:c.3412G>T	NP_004439.2:p.Glu1138Ter
NR_110535.1:n.3736G>T
XM_024450641.1:c.3550G>T	XP_024306409.1:p.Glu1184Ter
XM_024450642.1:c.3505G>T	XP_024306410.1:p.Glu1169Ter
XM_024450643.1:c.3460G>T	XP_024306411.1:p.Glu1154Ter
NM_001005862.3:c.3322G>T	NP_001005862.1:p.Glu1108Ter
NM_001289936.2:c.3367G>T	NP_001276865.1:p.Glu1123Ter
NM_001289937.2:c.3160-142G>T	NP_001276866.1:n.3160-142G>T
NM_001382782.1:c.3322G>T	NP_001369711.1:p.Glu1108Ter
NM_001382783.1:c.3322G>T	NP_001369712.1:p.Glu1108Ter
NM_001382784.1:c.3529G>T	NP_001369713.1:p.Glu1177Ter
NM_001382785.1:c.3514G>T	NP_001369714.1:p.Glu1172Ter
NM_001382786.1:c.3493G>T	NP_001369715.1:p.Glu1165Ter
NM_001382787.1:c.3487G>T	NP_001369716.1:p.Glu1163Ter
NM_001382788.1:c.3442G>T	NP_001369717.1:p.Glu1148Ter
NM_001382789.1:c.3433G>T	NP_001369718.1:p.Glu1145Ter
NM_001382790.1:c.3409G>T	NP_001369719.1:p.Glu1137Ter
NM_001382791.1:c.3403G>T	NP_001369720.1:p.Glu1135Ter
NM_001382792.1:c.3376G>T	NP_001369721.1:p.Glu1126Ter
NM_001382793.1:c.3370G>T	NP_001369722.1:p.Glu1124Ter
NM_001382794.1:c.3370G>T	NP_001369723.1:p.Glu1124Ter
NM_001382795.1:c.3364G>T	NP_001369724.1:p.Glu1122Ter
NM_001382796.1:c.3325G>T	NP_001369725.1:p.Glu1109Ter
NM_001382797.1:c.3313G>T	NP_001369726.1:p.Glu1105Ter
NM_001382798.1:c.3256G>T	NP_001369727.1:p.Glu1086Ter
NM_001382799.1:c.3232G>T	NP_001369728.1:p.Glu1078Ter
NM_001382800.1:c.3226G>T	NP_001369729.1:p.Glu1076Ter
NM_001382801.1:c.3208G>T	NP_001369730.1:p.Glu1070Ter
NM_001382802.1:c.3154G>T	NP_001369731.1:p.Glu1052Ter
NM_001382803.1:c.3118-142G>T	NP_001369732.1:n.3118-142G>T
NM_001382804.1:c.2584G>T	NP_001369733.1:p.Glu862Ter
NM_001382805.1:c.2461G>T	NP_001369734.1:p.Glu821Ter
NM_001382806.1:c.2374G>T	NP_001369735.1:p.Glu792Ter
NM_004448.4:c.3412G>T MANE Select	NP_004439.2:p.Glu1138Ter
NR_110535.2:n.3650G>T