Canonical Allele Identifier: CA499890487

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143288298
• MyVariant Identifiers: chr17:g.37883961T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727708T>C , CM000679.2:g.39727708T>C	GRCh38
NC_000017.10:g.37883961T>C , CM000679.1:g.37883961T>C	GRCh37
NC_000017.9:g.35137487T>C	NCBI36
NG_007503.1:g.44569T>C , LRG_724:g.44569T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3432T>C MANE Select	ENSP00000269571.4:p.Asp1144=
ENST00000269571.9:c.3432T>C	ENSP00000269571.4:p.Asp1144=
ENST00000406381.6:c.3342T>C	ENSP00000385185.2:p.Asp1114=
ENST00000445658.6:c.2604T>C	ENSP00000404047.2:p.Asp868=
ENST00000541774.5:c.3387T>C	ENSP00000446466.1:p.Asp1129=
ENST00000578373.5:c.*3222T>C	ENSP00000463427.1:n.*3222T>C
ENST00000584450.5:c.*11T>C	ENSP00000463714.1:n.*11T>C
ENST00000584601.5:c.3342T>C	ENSP00000462438.1:p.Asp1114=
NM_001005862.2:c.3342T>C , LRG_724t1:c.3342T>C	NP_001005862.1:p.Asp1114=
NM_001289936.1:c.3387T>C , LRG_724t4:c.3387T>C	NP_001276865.1:p.Asp1129=
NM_001289937.1:c.*11T>C	NP_001276866.1:n.*11T>C
NM_004448.3:c.3432T>C , LRG_724t2:c.3432T>C	NP_004439.2:p.Asp1144=
NR_110535.1:n.3756T>C
XM_024450641.1:c.3570T>C	XP_024306409.1:p.Asp1190=
XM_024450642.1:c.3525T>C	XP_024306410.1:p.Asp1175=
XM_024450643.1:c.3480T>C	XP_024306411.1:p.Asp1160=
NM_001005862.3:c.3342T>C	NP_001005862.1:p.Asp1114=
NM_001289936.2:c.3387T>C	NP_001276865.1:p.Asp1129=
NM_001289937.2:c.*11T>C	NP_001276866.1:n.*11T>C
NM_001382782.1:c.3342T>C	NP_001369711.1:p.Asp1114=
NM_001382783.1:c.3342T>C	NP_001369712.1:p.Asp1114=
NM_001382784.1:c.3549T>C	NP_001369713.1:p.Asp1183=
NM_001382785.1:c.3534T>C	NP_001369714.1:p.Asp1178=
NM_001382786.1:c.3513T>C	NP_001369715.1:p.Asp1171=
NM_001382787.1:c.3507T>C	NP_001369716.1:p.Asp1169=
NM_001382788.1:c.3462T>C	NP_001369717.1:p.Asp1154=
NM_001382789.1:c.3453T>C	NP_001369718.1:p.Asp1151=
NM_001382790.1:c.3429T>C	NP_001369719.1:p.Asp1143=
NM_001382791.1:c.3423T>C	NP_001369720.1:p.Asp1141=
NM_001382792.1:c.3396T>C	NP_001369721.1:p.Asp1132=
NM_001382793.1:c.3390T>C	NP_001369722.1:p.Asp1130=
NM_001382794.1:c.3390T>C	NP_001369723.1:p.Asp1130=
NM_001382795.1:c.3384T>C	NP_001369724.1:p.Asp1128=
NM_001382796.1:c.3345T>C	NP_001369725.1:p.Asp1115=
NM_001382797.1:c.3333T>C	NP_001369726.1:p.Asp1111=
NM_001382798.1:c.3276T>C	NP_001369727.1:p.Asp1092=
NM_001382799.1:c.3252T>C	NP_001369728.1:p.Asp1084=
NM_001382800.1:c.3246T>C	NP_001369729.1:p.Asp1082=
NM_001382801.1:c.3228T>C	NP_001369730.1:p.Asp1076=
NM_001382802.1:c.3174T>C	NP_001369731.1:p.Asp1058=
NM_001382803.1:c.*11T>C	NP_001369732.1:n.*11T>C
NM_001382804.1:c.2604T>C	NP_001369733.1:p.Asp868=
NM_001382805.1:c.2481T>C	NP_001369734.1:p.Asp827=
NM_001382806.1:c.2394T>C	NP_001369735.1:p.Asp798=
NM_004448.4:c.3432T>C MANE Select	NP_004439.2:p.Asp1144=
NR_110535.2:n.3670T>C