Canonical Allele Identifier: CA2840283116

Gene: ERBB2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39711890G>T , CM000679.2:g.39711890G>T	GRCh38
NC_000017.10:g.37868143G>T , CM000679.1:g.37868143G>T	GRCh37
NC_000017.9:g.35121669G>T	NCBI36
NG_007503.1:g.28751G>T , LRG_724:g.28751G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.902-38G>T MANE Select	ENSP00000269571.4:n.902-38G>T
ENST00000269571.9:c.902-38G>T	ENSP00000269571.4:n.902-38G>T
ENST00000406381.6:c.812-38G>T	ENSP00000385185.2:n.812-38G>T
ENST00000445658.6:c.74-38G>T	ENSP00000404047.2:n.74-38G>T
ENST00000541774.5:c.857-38G>T	ENSP00000446466.1:n.857-38G>T
ENST00000578199.5:c.812-38G>T	ENSP00000462808.1:n.812-38G>T
ENST00000578373.5:c.*692-38G>T	ENSP00000463427.1:n.*692-38G>T
ENST00000578502.1:c.127-38G>T
ENST00000582648.5:c.226-38G>T	ENSP00000462024.1:n.226-38G>T
ENST00000582788.5:n.391-38G>T
ENST00000583038.5:n.1594-38G>T
ENST00000584450.5:c.902-38G>T	ENSP00000463714.1:n.902-38G>T
ENST00000584601.5:c.812-38G>T	ENSP00000462438.1:n.812-38G>T
ENST00000584908.5:n.914-38G>T
NM_001005862.2:c.812-38G>T , LRG_724t1:c.812-38G>T	NP_001005862.1:n.812-38G>T
NM_001289936.1:c.857-38G>T , LRG_724t4:c.857-38G>T	NP_001276865.1:n.857-38G>T
NM_001289937.1:c.902-38G>T	NP_001276866.1:n.902-38G>T
NM_001289938.1:c.812-38G>T , LRG_724t3:c.812-38G>T	NP_001276867.1:n.812-38G>T
NM_004448.3:c.902-38G>T , LRG_724t2:c.902-38G>T	NP_004439.2:n.902-38G>T
NR_110535.1:n.1226-38G>T
XM_024450641.1:c.1040-38G>T	XP_024306409.1:n.1040-38G>T
XM_024450642.1:c.995-38G>T	XP_024306410.1:n.995-38G>T
XM_024450643.1:c.950-38G>T	XP_024306411.1:n.950-38G>T
NM_001005862.3:c.812-38G>T	NP_001005862.1:n.812-38G>T
NM_001289936.2:c.857-38G>T	NP_001276865.1:n.857-38G>T
NM_001289937.2:c.902-38G>T	NP_001276866.1:n.902-38G>T
NM_001289938.2:c.812-38G>T	NP_001276867.1:n.812-38G>T
NM_001382782.1:c.812-38G>T	NP_001369711.1:n.812-38G>T
NM_001382783.1:c.812-38G>T	NP_001369712.1:n.812-38G>T
NM_001382784.1:c.902-38G>T	NP_001369713.1:n.902-38G>T
NM_001382785.1:c.902-38G>T	NP_001369714.1:n.902-38G>T
NM_001382786.1:c.902-38G>T	NP_001369715.1:n.902-38G>T
NM_001382787.1:c.977-38G>T	NP_001369716.1:n.977-38G>T
NM_001382788.1:c.902-38G>T	NP_001369717.1:n.902-38G>T
NM_001382789.1:c.902-38G>T	NP_001369718.1:n.902-38G>T
NM_001382790.1:c.902-38G>T	NP_001369719.1:n.902-38G>T
NM_001382791.1:c.893-38G>T	NP_001369720.1:n.893-38G>T
NM_001382792.1:c.902-38G>T	NP_001369721.1:n.902-38G>T
NM_001382793.1:c.902-38G>T	NP_001369722.1:n.902-38G>T
NM_001382794.1:c.902-38G>T	NP_001369723.1:n.902-38G>T
NM_001382795.1:c.902-38G>T	NP_001369724.1:n.902-38G>T
NM_001382796.1:c.902-38G>T	NP_001369725.1:n.902-38G>T
NM_001382797.1:c.902-38G>T	NP_001369726.1:n.902-38G>T
NM_001382798.1:c.902-38G>T	NP_001369727.1:n.902-38G>T
NM_001382799.1:c.722-38G>T	NP_001369728.1:n.722-38G>T
NM_001382800.1:c.902-38G>T	NP_001369729.1:n.902-38G>T
NM_001382801.1:c.902-38G>T	NP_001369730.1:n.902-38G>T
NM_001382802.1:c.644-38G>T	NP_001369731.1:n.644-38G>T
NM_001382803.1:c.902-38G>T	NP_001369732.1:n.902-38G>T
NM_001382804.1:c.74-38G>T	NP_001369733.1:n.74-38G>T
NM_001382805.1:c.902-38G>T	NP_001369734.1:n.902-38G>T
NM_001382806.1:c.902-38G>T	NP_001369735.1:n.902-38G>T
NM_004448.4:c.902-38G>T MANE Select	NP_004439.2:n.902-38G>T
NR_110535.2:n.1140-38G>T