Canonical Allele Identifier: CA499890589

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37884003T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727750T>A , CM000679.2:g.39727750T>A	GRCh38
NC_000017.10:g.37884003T>A , CM000679.1:g.37884003T>A	GRCh37
NC_000017.9:g.35137529T>A	NCBI36
NG_007503.1:g.44611T>A , LRG_724:g.44611T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3474T>A MANE Select	ENSP00000269571.4:p.Pro1158=
ENST00000269571.9:c.3474T>A	ENSP00000269571.4:p.Pro1158=
ENST00000406381.6:c.3384T>A	ENSP00000385185.2:p.Pro1128=
ENST00000445658.6:c.2646T>A	ENSP00000404047.2:p.Pro882=
ENST00000541774.5:c.3429T>A	ENSP00000446466.1:p.Pro1143=
ENST00000578373.5:c.*3264T>A	ENSP00000463427.1:n.*3264T>A
ENST00000584450.5:c.*53T>A	ENSP00000463714.1:n.*53T>A
ENST00000584601.5:c.3384T>A	ENSP00000462438.1:p.Pro1128=
NM_001005862.2:c.3384T>A , LRG_724t1:c.3384T>A	NP_001005862.1:p.Pro1128=
NM_001289936.1:c.3429T>A , LRG_724t4:c.3429T>A	NP_001276865.1:p.Pro1143=
NM_001289937.1:c.*53T>A	NP_001276866.1:n.*53T>A
NM_004448.3:c.3474T>A , LRG_724t2:c.3474T>A	NP_004439.2:p.Pro1158=
NR_110535.1:n.3798T>A
XM_024450641.1:c.3612T>A	XP_024306409.1:p.Pro1204=
XM_024450642.1:c.3567T>A	XP_024306410.1:p.Pro1189=
XM_024450643.1:c.3522T>A	XP_024306411.1:p.Pro1174=
NM_001005862.3:c.3384T>A	NP_001005862.1:p.Pro1128=
NM_001289936.2:c.3429T>A	NP_001276865.1:p.Pro1143=
NM_001289937.2:c.*53T>A	NP_001276866.1:n.*53T>A
NM_001382782.1:c.3384T>A	NP_001369711.1:p.Pro1128=
NM_001382783.1:c.3384T>A	NP_001369712.1:p.Pro1128=
NM_001382784.1:c.3591T>A	NP_001369713.1:p.Pro1197=
NM_001382785.1:c.3576T>A	NP_001369714.1:p.Pro1192=
NM_001382786.1:c.3555T>A	NP_001369715.1:p.Pro1185=
NM_001382787.1:c.3549T>A	NP_001369716.1:p.Pro1183=
NM_001382788.1:c.3504T>A	NP_001369717.1:p.Pro1168=
NM_001382789.1:c.3495T>A	NP_001369718.1:p.Pro1165=
NM_001382790.1:c.3471T>A	NP_001369719.1:p.Pro1157=
NM_001382791.1:c.3465T>A	NP_001369720.1:p.Pro1155=
NM_001382792.1:c.3438T>A	NP_001369721.1:p.Pro1146=
NM_001382793.1:c.3432T>A	NP_001369722.1:p.Pro1144=
NM_001382794.1:c.3432T>A	NP_001369723.1:p.Pro1144=
NM_001382795.1:c.3426T>A	NP_001369724.1:p.Pro1142=
NM_001382796.1:c.3387T>A	NP_001369725.1:p.Pro1129=
NM_001382797.1:c.3375T>A	NP_001369726.1:p.Pro1125=
NM_001382798.1:c.3318T>A	NP_001369727.1:p.Pro1106=
NM_001382799.1:c.3294T>A	NP_001369728.1:p.Pro1098=
NM_001382800.1:c.3288T>A	NP_001369729.1:p.Pro1096=
NM_001382801.1:c.3270T>A	NP_001369730.1:p.Pro1090=
NM_001382802.1:c.3216T>A	NP_001369731.1:p.Pro1072=
NM_001382803.1:c.*53T>A	NP_001369732.1:n.*53T>A
NM_001382804.1:c.2646T>A	NP_001369733.1:p.Pro882=
NM_001382805.1:c.2523T>A	NP_001369734.1:p.Pro841=
NM_001382806.1:c.2436T>A	NP_001369735.1:p.Pro812=
NM_004448.4:c.3474T>A MANE Select	NP_004439.2:p.Pro1158=
NR_110535.2:n.3712T>A