Canonical Allele Identifier: CA2259228011

Gene: ERBB2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39724803G= , CM000679.2:g.39724803G=	GRCh38
NC_000017.10:g.37881056G= , CM000679.1:g.37881056G=	GRCh37
NC_000017.9:g.35134582G=	NCBI36
NG_007503.1:g.41664G= , LRG_724:g.41664G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.2385G= MANE Select	ENSP00000269571.4:p.Gln795=
ENST00000269571.9:c.2385G=	ENSP00000269571.4:p.Gln795=
ENST00000406381.6:c.2295G=	ENSP00000385185.2:p.Gln765=
ENST00000445658.6:c.1557G=	ENSP00000404047.2:p.Gln519=
ENST00000541774.5:c.2340G=	ENSP00000446466.1:p.Gln780=
ENST00000578373.5:c.*2175G=	ENSP00000463427.1:n.*2175G=
ENST00000580074.1:c.491G=
ENST00000583038.5:n.3519G=
ENST00000584450.5:c.2385G=	ENSP00000463714.1:p.Gln795=
ENST00000584601.5:c.2295G=	ENSP00000462438.1:p.Gln765=
NM_001005862.2:c.2295G= , LRG_724t1:c.2295G=	NP_001005862.1:p.Gln765=
NM_001289936.1:c.2340G= , LRG_724t4:c.2340G=	NP_001276865.1:p.Gln780=
NM_001289937.1:c.2385G=	NP_001276866.1:p.Gln795=
NM_004448.3:c.2385G= , LRG_724t2:c.2385G=	NP_004439.2:p.Gln795=
NR_110535.1:n.2709G=
XM_024450641.1:c.2523G=	XP_024306409.1:p.Gln841=
XM_024450642.1:c.2478G=	XP_024306410.1:p.Gln826=
XM_024450643.1:c.2433G=	XP_024306411.1:p.Gln811=
NM_001005862.3:c.2295G=	NP_001005862.1:p.Gln765=
NM_001289936.2:c.2340G=	NP_001276865.1:p.Gln780=
NM_001289937.2:c.2385G=	NP_001276866.1:p.Gln795=
NM_001382782.1:c.2295G=	NP_001369711.1:p.Gln765=
NM_001382783.1:c.2295G=	NP_001369712.1:p.Gln765=
NM_001382784.1:c.2502G=	NP_001369713.1:p.Gln834=
NM_001382785.1:c.2487G=	NP_001369714.1:p.Gln829=
NM_001382786.1:c.2466G=	NP_001369715.1:p.Gln822=
NM_001382787.1:c.2460G=	NP_001369716.1:p.Gln820=
NM_001382788.1:c.2415G=	NP_001369717.1:p.Gln805=
NM_001382789.1:c.2406G=	NP_001369718.1:p.Gln802=
NM_001382790.1:c.2382G=	NP_001369719.1:p.Gln794=
NM_001382791.1:c.2376G=	NP_001369720.1:p.Gln792=
NM_001382792.1:c.2349G=	NP_001369721.1:p.Gln783=
NM_001382793.1:c.2343G=	NP_001369722.1:p.Gln781=
NM_001382794.1:c.2343G=	NP_001369723.1:p.Gln781=
NM_001382795.1:c.2337G=	NP_001369724.1:p.Gln779=
NM_001382796.1:c.2385G=	NP_001369725.1:p.Gln795=
NM_001382797.1:c.2286G=	NP_001369726.1:p.Gln762=
NM_001382798.1:c.2385G=	NP_001369727.1:p.Gln795=
NM_001382799.1:c.2205G=	NP_001369728.1:p.Gln735=
NM_001382800.1:c.2308-246G=	NP_001369729.1:n.2308-246G=
NM_001382801.1:c.2337G=	NP_001369730.1:p.Gln779=
NM_001382802.1:c.2127G=	NP_001369731.1:p.Gln709=
NM_001382803.1:c.2343G=	NP_001369732.1:p.Gln781=
NM_001382804.1:c.1557G=	NP_001369733.1:p.Gln519=
NM_001382805.1:c.2208+1143G=	NP_001369734.1:n.2208+1143G=
NM_001382806.1:c.1347G=	NP_001369735.1:p.Gln449=
NM_004448.4:c.2385G= MANE Select	NP_004439.2:p.Gln795=
NR_110535.2:n.2623G=