Canonical Allele Identifier: CA290443982

Gene: ERBB2

Linked Data

• dbSNP Id: rs182815010
• MyVariant Identifiers: chr17:g.37884103G>T (hg19) ; chr17:g.39727850G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727850G>T , CM000679.2:g.39727850G>T	GRCh38
NC_000017.10:g.37884103G>T , CM000679.1:g.37884103G>T	GRCh37
NC_000017.9:g.35137629G>T	NCBI36
NG_007503.1:g.44711G>T , LRG_724:g.44711G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3574G>T MANE Select	ENSP00000269571.4:p.Glu1192Ter
ENST00000269571.9:c.3574G>T	ENSP00000269571.4:p.Glu1192Ter
ENST00000406381.6:c.3484G>T	ENSP00000385185.2:p.Glu1162Ter
ENST00000445658.6:c.2746G>T	ENSP00000404047.2:p.Glu916Ter
ENST00000541774.5:c.3529G>T	ENSP00000446466.1:p.Glu1177Ter
ENST00000578373.5:c.*3364G>T	ENSP00000463427.1:n.*3364G>T
ENST00000584450.5:c.*153G>T	ENSP00000463714.1:n.*153G>T
ENST00000584601.5:c.3484G>T	ENSP00000462438.1:p.Glu1162Ter
NM_001005862.2:c.3484G>T , LRG_724t1:c.3484G>T	NP_001005862.1:p.Glu1162Ter
NM_001289936.1:c.3529G>T , LRG_724t4:c.3529G>T	NP_001276865.1:p.Glu1177Ter
NM_001289937.1:c.*153G>T	NP_001276866.1:n.*153G>T
NM_004448.3:c.3574G>T , LRG_724t2:c.3574G>T	NP_004439.2:p.Glu1192Ter
NR_110535.1:n.3898G>T
XM_024450641.1:c.3712G>T	XP_024306409.1:p.Glu1238Ter
XM_024450642.1:c.3667G>T	XP_024306410.1:p.Glu1223Ter
XM_024450643.1:c.3622G>T	XP_024306411.1:p.Glu1208Ter
NM_001005862.3:c.3484G>T	NP_001005862.1:p.Glu1162Ter
NM_001289936.2:c.3529G>T	NP_001276865.1:p.Glu1177Ter
NM_001289937.2:c.*153G>T	NP_001276866.1:n.*153G>T
NM_001382782.1:c.3484G>T	NP_001369711.1:p.Glu1162Ter
NM_001382783.1:c.3484G>T	NP_001369712.1:p.Glu1162Ter
NM_001382784.1:c.3691G>T	NP_001369713.1:p.Glu1231Ter
NM_001382785.1:c.3676G>T	NP_001369714.1:p.Glu1226Ter
NM_001382786.1:c.3655G>T	NP_001369715.1:p.Glu1219Ter
NM_001382787.1:c.3649G>T	NP_001369716.1:p.Glu1217Ter
NM_001382788.1:c.3604G>T	NP_001369717.1:p.Glu1202Ter
NM_001382789.1:c.3595G>T	NP_001369718.1:p.Glu1199Ter
NM_001382790.1:c.3571G>T	NP_001369719.1:p.Glu1191Ter
NM_001382791.1:c.3565G>T	NP_001369720.1:p.Glu1189Ter
NM_001382792.1:c.3538G>T	NP_001369721.1:p.Glu1180Ter
NM_001382793.1:c.3532G>T	NP_001369722.1:p.Glu1178Ter
NM_001382794.1:c.3532G>T	NP_001369723.1:p.Glu1178Ter
NM_001382795.1:c.3526G>T	NP_001369724.1:p.Glu1176Ter
NM_001382796.1:c.3487G>T	NP_001369725.1:p.Glu1163Ter
NM_001382797.1:c.3475G>T	NP_001369726.1:p.Glu1159Ter
NM_001382798.1:c.3418G>T	NP_001369727.1:p.Glu1140Ter
NM_001382799.1:c.3394G>T	NP_001369728.1:p.Glu1132Ter
NM_001382800.1:c.3388G>T	NP_001369729.1:p.Glu1130Ter
NM_001382801.1:c.3370G>T	NP_001369730.1:p.Glu1124Ter
NM_001382802.1:c.3316G>T	NP_001369731.1:p.Glu1106Ter
NM_001382803.1:c.*153G>T	NP_001369732.1:n.*153G>T
NM_001382804.1:c.2746G>T	NP_001369733.1:p.Glu916Ter
NM_001382805.1:c.2623G>T	NP_001369734.1:p.Glu875Ter
NM_001382806.1:c.2536G>T	NP_001369735.1:p.Glu846Ter
NM_004448.4:c.3574G>T MANE Select	NP_004439.2:p.Glu1192Ter
NR_110535.2:n.3812G>T