Canonical Allele Identifier: CA2259228039

Gene: ERBB2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39724877A= , CM000679.2:g.39724877A=	GRCh38
NC_000017.10:g.37881130A= , CM000679.1:g.37881130A=	GRCh37
NC_000017.9:g.35134656A=	NCBI36
NG_007503.1:g.41738A= , LRG_724:g.41738A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.2459A= MANE Select	ENSP00000269571.4:p.Gln820=
ENST00000269571.9:c.2459A=	ENSP00000269571.4:p.Gln820=
ENST00000406381.6:c.2369A=	ENSP00000385185.2:p.Gln790=
ENST00000445658.6:c.1631A=	ENSP00000404047.2:p.Gln544=
ENST00000541774.5:c.2414A=	ENSP00000446466.1:p.Gln805=
ENST00000578373.5:c.*2249A=	ENSP00000463427.1:n.*2249A=
ENST00000580074.1:c.565A=
ENST00000583038.5:n.3593A=
ENST00000584450.5:c.2459A=	ENSP00000463714.1:p.Gln820=
ENST00000584601.5:c.2369A=	ENSP00000462438.1:p.Gln790=
NM_001005862.2:c.2369A= , LRG_724t1:c.2369A=	NP_001005862.1:p.Gln790=
NM_001289936.1:c.2414A= , LRG_724t4:c.2414A=	NP_001276865.1:p.Gln805=
NM_001289937.1:c.2459A=	NP_001276866.1:p.Gln820=
NM_004448.3:c.2459A= , LRG_724t2:c.2459A=	NP_004439.2:p.Gln820=
NR_110535.1:n.2783A=
XM_024450641.1:c.2597A=	XP_024306409.1:p.Gln866=
XM_024450642.1:c.2552A=	XP_024306410.1:p.Gln851=
XM_024450643.1:c.2507A=	XP_024306411.1:p.Gln836=
NM_001005862.3:c.2369A=	NP_001005862.1:p.Gln790=
NM_001289936.2:c.2414A=	NP_001276865.1:p.Gln805=
NM_001289937.2:c.2459A=	NP_001276866.1:p.Gln820=
NM_001382782.1:c.2369A=	NP_001369711.1:p.Gln790=
NM_001382783.1:c.2369A=	NP_001369712.1:p.Gln790=
NM_001382784.1:c.2576A=	NP_001369713.1:p.Gln859=
NM_001382785.1:c.2561A=	NP_001369714.1:p.Gln854=
NM_001382786.1:c.2540A=	NP_001369715.1:p.Gln847=
NM_001382787.1:c.2534A=	NP_001369716.1:p.Gln845=
NM_001382788.1:c.2489A=	NP_001369717.1:p.Gln830=
NM_001382789.1:c.2480A=	NP_001369718.1:p.Gln827=
NM_001382790.1:c.2456A=	NP_001369719.1:p.Gln819=
NM_001382791.1:c.2450A=	NP_001369720.1:p.Gln817=
NM_001382792.1:c.2423A=	NP_001369721.1:p.Gln808=
NM_001382793.1:c.2417A=	NP_001369722.1:p.Gln806=
NM_001382794.1:c.2417A=	NP_001369723.1:p.Gln806=
NM_001382795.1:c.2411A=	NP_001369724.1:p.Gln804=
NM_001382796.1:c.2459A=	NP_001369725.1:p.Gln820=
NM_001382797.1:c.2360A=	NP_001369726.1:p.Gln787=
NM_001382798.1:c.2459A=	NP_001369727.1:p.Gln820=
NM_001382799.1:c.2279A=	NP_001369728.1:p.Gln760=
NM_001382800.1:c.2308-172A=	NP_001369729.1:n.2308-172A=
NM_001382801.1:c.2411A=	NP_001369730.1:p.Gln804=
NM_001382802.1:c.2201A=	NP_001369731.1:p.Gln734=
NM_001382803.1:c.2417A=	NP_001369732.1:p.Gln806=
NM_001382804.1:c.1631A=	NP_001369733.1:p.Gln544=
NM_001382805.1:c.2208+1217A=	NP_001369734.1:n.2208+1217A=
NM_001382806.1:c.1421A=	NP_001369735.1:p.Gln474=
NM_004448.4:c.2459A= MANE Select	NP_004439.2:p.Gln820=
NR_110535.2:n.2697A=