Canonical Allele Identifier: CA2259229138

Gene: ERBB2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727507T= , CM000679.2:g.39727507T=	GRCh38
NC_000017.10:g.37883760T= , CM000679.1:g.37883760T=	GRCh37
NC_000017.9:g.35137286T=	NCBI36
NG_007503.1:g.44368T= , LRG_724:g.44368T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3372T= MANE Select	ENSP00000269571.4:p.Thr1124=
ENST00000269571.9:c.3372T=	ENSP00000269571.4:p.Thr1124=
ENST00000406381.6:c.3282T=	ENSP00000385185.2:p.Thr1094=
ENST00000445658.6:c.2544T=	ENSP00000404047.2:p.Thr848=
ENST00000541774.5:c.3327T=	ENSP00000446466.1:p.Thr1109=
ENST00000578373.5:c.*3162T=	ENSP00000463427.1:n.*3162T=
ENST00000584450.5:c.3160-182T=	ENSP00000463714.1:n.3160-182T=
ENST00000584601.5:c.3282T=	ENSP00000462438.1:p.Thr1094=
NM_001005862.2:c.3282T= , LRG_724t1:c.3282T=	NP_001005862.1:p.Thr1094=
NM_001289936.1:c.3327T= , LRG_724t4:c.3327T=	NP_001276865.1:p.Thr1109=
NM_001289937.1:c.3160-182T=	NP_001276866.1:n.3160-182T=
NM_004448.3:c.3372T= , LRG_724t2:c.3372T=	NP_004439.2:p.Thr1124=
NR_110535.1:n.3696T=
XM_024450641.1:c.3510T=	XP_024306409.1:p.Thr1170=
XM_024450642.1:c.3465T=	XP_024306410.1:p.Thr1155=
XM_024450643.1:c.3420T=	XP_024306411.1:p.Thr1140=
NM_001005862.3:c.3282T=	NP_001005862.1:p.Thr1094=
NM_001289936.2:c.3327T=	NP_001276865.1:p.Thr1109=
NM_001289937.2:c.3160-182T=	NP_001276866.1:n.3160-182T=
NM_001382782.1:c.3282T=	NP_001369711.1:p.Thr1094=
NM_001382783.1:c.3282T=	NP_001369712.1:p.Thr1094=
NM_001382784.1:c.3489T=	NP_001369713.1:p.Thr1163=
NM_001382785.1:c.3474T=	NP_001369714.1:p.Thr1158=
NM_001382786.1:c.3453T=	NP_001369715.1:p.Thr1151=
NM_001382787.1:c.3447T=	NP_001369716.1:p.Thr1149=
NM_001382788.1:c.3402T=	NP_001369717.1:p.Thr1134=
NM_001382789.1:c.3393T=	NP_001369718.1:p.Thr1131=
NM_001382790.1:c.3369T=	NP_001369719.1:p.Thr1123=
NM_001382791.1:c.3363T=	NP_001369720.1:p.Thr1121=
NM_001382792.1:c.3336T=	NP_001369721.1:p.Thr1112=
NM_001382793.1:c.3330T=	NP_001369722.1:p.Thr1110=
NM_001382794.1:c.3330T=	NP_001369723.1:p.Thr1110=
NM_001382795.1:c.3324T=	NP_001369724.1:p.Thr1108=
NM_001382796.1:c.3285T=	NP_001369725.1:p.Thr1095=
NM_001382797.1:c.3273T=	NP_001369726.1:p.Thr1091=
NM_001382798.1:c.3216T=	NP_001369727.1:p.Thr1072=
NM_001382799.1:c.3192T=	NP_001369728.1:p.Thr1064=
NM_001382800.1:c.3186T=	NP_001369729.1:p.Thr1062=
NM_001382801.1:c.3168T=	NP_001369730.1:p.Thr1056=
NM_001382802.1:c.3114T=	NP_001369731.1:p.Thr1038=
NM_001382803.1:c.3118-182T=	NP_001369732.1:n.3118-182T=
NM_001382804.1:c.2544T=	NP_001369733.1:p.Thr848=
NM_001382805.1:c.2421T=	NP_001369734.1:p.Thr807=
NM_001382806.1:c.2334T=	NP_001369735.1:p.Thr778=
NM_004448.4:c.3372T= MANE Select	NP_004439.2:p.Thr1124=
NR_110535.2:n.3610T=