Canonical Allele Identifier: CA2259229301

Gene: ERBB2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727880G= , CM000679.2:g.39727880G=	GRCh38
NC_000017.10:g.37884133G= , CM000679.1:g.37884133G=	GRCh37
NC_000017.9:g.35137659G=	NCBI36
NG_007503.1:g.44741G= , LRG_724:g.44741G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3604G= MANE Select	ENSP00000269571.4:p.Gly1202=
ENST00000269571.9:c.3604G=	ENSP00000269571.4:p.Gly1202=
ENST00000406381.6:c.3514G=	ENSP00000385185.2:p.Gly1172=
ENST00000445658.6:c.2776G=	ENSP00000404047.2:p.Gly926=
ENST00000541774.5:c.3559G=	ENSP00000446466.1:p.Gly1187=
ENST00000578373.5:c.*3394G=	ENSP00000463427.1:n.*3394G=
ENST00000584450.5:c.*183G=	ENSP00000463714.1:n.*183G=
ENST00000584601.5:c.3514G=	ENSP00000462438.1:p.Gly1172=
NM_001005862.2:c.3514G= , LRG_724t1:c.3514G=	NP_001005862.1:p.Gly1172=
NM_001289936.1:c.3559G= , LRG_724t4:c.3559G=	NP_001276865.1:p.Gly1187=
NM_001289937.1:c.*183G=	NP_001276866.1:n.*183G=
NM_004448.3:c.3604G= , LRG_724t2:c.3604G=	NP_004439.2:p.Gly1202=
NR_110535.1:n.3928G=
XM_024450641.1:c.3742G=	XP_024306409.1:p.Gly1248=
XM_024450642.1:c.3697G=	XP_024306410.1:p.Gly1233=
XM_024450643.1:c.3652G=	XP_024306411.1:p.Gly1218=
NM_001005862.3:c.3514G=	NP_001005862.1:p.Gly1172=
NM_001289936.2:c.3559G=	NP_001276865.1:p.Gly1187=
NM_001289937.2:c.*183G=	NP_001276866.1:n.*183G=
NM_001382782.1:c.3514G=	NP_001369711.1:p.Gly1172=
NM_001382783.1:c.3514G=	NP_001369712.1:p.Gly1172=
NM_001382784.1:c.3721G=	NP_001369713.1:p.Gly1241=
NM_001382785.1:c.3706G=	NP_001369714.1:p.Gly1236=
NM_001382786.1:c.3685G=	NP_001369715.1:p.Gly1229=
NM_001382787.1:c.3679G=	NP_001369716.1:p.Gly1227=
NM_001382788.1:c.3634G=	NP_001369717.1:p.Gly1212=
NM_001382789.1:c.3625G=	NP_001369718.1:p.Gly1209=
NM_001382790.1:c.3601G=	NP_001369719.1:p.Gly1201=
NM_001382791.1:c.3595G=	NP_001369720.1:p.Gly1199=
NM_001382792.1:c.3568G=	NP_001369721.1:p.Gly1190=
NM_001382793.1:c.3562G=	NP_001369722.1:p.Gly1188=
NM_001382794.1:c.3562G=	NP_001369723.1:p.Gly1188=
NM_001382795.1:c.3556G=	NP_001369724.1:p.Gly1186=
NM_001382796.1:c.3517G=	NP_001369725.1:p.Gly1173=
NM_001382797.1:c.3505G=	NP_001369726.1:p.Gly1169=
NM_001382798.1:c.3448G=	NP_001369727.1:p.Gly1150=
NM_001382799.1:c.3424G=	NP_001369728.1:p.Gly1142=
NM_001382800.1:c.3418G=	NP_001369729.1:p.Gly1140=
NM_001382801.1:c.3400G=	NP_001369730.1:p.Gly1134=
NM_001382802.1:c.3346G=	NP_001369731.1:p.Gly1116=
NM_001382803.1:c.*183G=	NP_001369732.1:n.*183G=
NM_001382804.1:c.2776G=	NP_001369733.1:p.Gly926=
NM_001382805.1:c.2653G=	NP_001369734.1:p.Gly885=
NM_001382806.1:c.2566G=	NP_001369735.1:p.Gly856=
NM_004448.4:c.3604G= MANE Select	NP_004439.2:p.Gly1202=
NR_110535.2:n.3842G=