Canonical Allele Identifier: CA399312592

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37883730G>T (hg19) ; chr17:g.39727477G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727477G>T , CM000679.2:g.39727477G>T	GRCh38
NC_000017.10:g.37883730G>T , CM000679.1:g.37883730G>T	GRCh37
NC_000017.9:g.35137256G>T	NCBI36
NG_007503.1:g.44338G>T , LRG_724:g.44338G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3342G>T MANE Select	ENSP00000269571.4:p.Glu1114Asp
ENST00000269571.9:c.3342G>T	ENSP00000269571.4:p.Glu1114Asp
ENST00000406381.6:c.3252G>T	ENSP00000385185.2:p.Glu1084Asp
ENST00000445658.6:c.2514G>T	ENSP00000404047.2:p.Glu838Asp
ENST00000541774.5:c.3297G>T	ENSP00000446466.1:p.Glu1099Asp
ENST00000578373.5:c.*3132G>T	ENSP00000463427.1:n.*3132G>T
ENST00000584450.5:c.3160-212G>T	ENSP00000463714.1:n.3160-212G>T
ENST00000584601.5:c.3252G>T	ENSP00000462438.1:p.Glu1084Asp
NM_001005862.2:c.3252G>T , LRG_724t1:c.3252G>T	NP_001005862.1:p.Glu1084Asp
NM_001289936.1:c.3297G>T , LRG_724t4:c.3297G>T	NP_001276865.1:p.Glu1099Asp
NM_001289937.1:c.3160-212G>T	NP_001276866.1:n.3160-212G>T
NM_004448.3:c.3342G>T , LRG_724t2:c.3342G>T	NP_004439.2:p.Glu1114Asp
NR_110535.1:n.3666G>T
XM_024450641.1:c.3480G>T	XP_024306409.1:p.Glu1160Asp
XM_024450642.1:c.3435G>T	XP_024306410.1:p.Glu1145Asp
XM_024450643.1:c.3390G>T	XP_024306411.1:p.Glu1130Asp
NM_001005862.3:c.3252G>T	NP_001005862.1:p.Glu1084Asp
NM_001289936.2:c.3297G>T	NP_001276865.1:p.Glu1099Asp
NM_001289937.2:c.3160-212G>T	NP_001276866.1:n.3160-212G>T
NM_001382782.1:c.3252G>T	NP_001369711.1:p.Glu1084Asp
NM_001382783.1:c.3252G>T	NP_001369712.1:p.Glu1084Asp
NM_001382784.1:c.3459G>T	NP_001369713.1:p.Glu1153Asp
NM_001382785.1:c.3444G>T	NP_001369714.1:p.Glu1148Asp
NM_001382786.1:c.3423G>T	NP_001369715.1:p.Glu1141Asp
NM_001382787.1:c.3417G>T	NP_001369716.1:p.Glu1139Asp
NM_001382788.1:c.3372G>T	NP_001369717.1:p.Glu1124Asp
NM_001382789.1:c.3363G>T	NP_001369718.1:p.Glu1121Asp
NM_001382790.1:c.3339G>T	NP_001369719.1:p.Glu1113Asp
NM_001382791.1:c.3333G>T	NP_001369720.1:p.Glu1111Asp
NM_001382792.1:c.3306G>T	NP_001369721.1:p.Glu1102Asp
NM_001382793.1:c.3300G>T	NP_001369722.1:p.Glu1100Asp
NM_001382794.1:c.3300G>T	NP_001369723.1:p.Glu1100Asp
NM_001382795.1:c.3294G>T	NP_001369724.1:p.Glu1098Asp
NM_001382796.1:c.3255G>T	NP_001369725.1:p.Glu1085Asp
NM_001382797.1:c.3243G>T	NP_001369726.1:p.Glu1081Asp
NM_001382798.1:c.3186G>T	NP_001369727.1:p.Glu1062Asp
NM_001382799.1:c.3162G>T	NP_001369728.1:p.Glu1054Asp
NM_001382800.1:c.3156G>T	NP_001369729.1:p.Glu1052Asp
NM_001382801.1:c.3138G>T	NP_001369730.1:p.Glu1046Asp
NM_001382802.1:c.3084G>T	NP_001369731.1:p.Glu1028Asp
NM_001382803.1:c.3118-212G>T	NP_001369732.1:n.3118-212G>T
NM_001382804.1:c.2514G>T	NP_001369733.1:p.Glu838Asp
NM_001382805.1:c.2391G>T	NP_001369734.1:p.Glu797Asp
NM_001382806.1:c.2304G>T	NP_001369735.1:p.Glu768Asp
NM_004448.4:c.3342G>T MANE Select	NP_004439.2:p.Glu1114Asp
NR_110535.2:n.3580G>T