Canonical Allele Identifier: CA399313691

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143303875
• MyVariant Identifiers: chr17:g.37884104A>T (hg19) ; chr17:g.39727851A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727851A>T , CM000679.2:g.39727851A>T	GRCh38
NC_000017.10:g.37884104A>T , CM000679.1:g.37884104A>T	GRCh37
NC_000017.9:g.35137630A>T	NCBI36
NG_007503.1:g.44712A>T , LRG_724:g.44712A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3575A>T MANE Select	ENSP00000269571.4:p.Glu1192Val
ENST00000269571.9:c.3575A>T	ENSP00000269571.4:p.Glu1192Val
ENST00000406381.6:c.3485A>T	ENSP00000385185.2:p.Glu1162Val
ENST00000445658.6:c.2747A>T	ENSP00000404047.2:p.Glu916Val
ENST00000541774.5:c.3530A>T	ENSP00000446466.1:p.Glu1177Val
ENST00000578373.5:c.*3365A>T	ENSP00000463427.1:n.*3365A>T
ENST00000584450.5:c.*154A>T	ENSP00000463714.1:n.*154A>T
ENST00000584601.5:c.3485A>T	ENSP00000462438.1:p.Glu1162Val
NM_001005862.2:c.3485A>T , LRG_724t1:c.3485A>T	NP_001005862.1:p.Glu1162Val
NM_001289936.1:c.3530A>T , LRG_724t4:c.3530A>T	NP_001276865.1:p.Glu1177Val
NM_001289937.1:c.*154A>T	NP_001276866.1:n.*154A>T
NM_004448.3:c.3575A>T , LRG_724t2:c.3575A>T	NP_004439.2:p.Glu1192Val
NR_110535.1:n.3899A>T
XM_024450641.1:c.3713A>T	XP_024306409.1:p.Glu1238Val
XM_024450642.1:c.3668A>T	XP_024306410.1:p.Glu1223Val
XM_024450643.1:c.3623A>T	XP_024306411.1:p.Glu1208Val
NM_001005862.3:c.3485A>T	NP_001005862.1:p.Glu1162Val
NM_001289936.2:c.3530A>T	NP_001276865.1:p.Glu1177Val
NM_001289937.2:c.*154A>T	NP_001276866.1:n.*154A>T
NM_001382782.1:c.3485A>T	NP_001369711.1:p.Glu1162Val
NM_001382783.1:c.3485A>T	NP_001369712.1:p.Glu1162Val
NM_001382784.1:c.3692A>T	NP_001369713.1:p.Glu1231Val
NM_001382785.1:c.3677A>T	NP_001369714.1:p.Glu1226Val
NM_001382786.1:c.3656A>T	NP_001369715.1:p.Glu1219Val
NM_001382787.1:c.3650A>T	NP_001369716.1:p.Glu1217Val
NM_001382788.1:c.3605A>T	NP_001369717.1:p.Glu1202Val
NM_001382789.1:c.3596A>T	NP_001369718.1:p.Glu1199Val
NM_001382790.1:c.3572A>T	NP_001369719.1:p.Glu1191Val
NM_001382791.1:c.3566A>T	NP_001369720.1:p.Glu1189Val
NM_001382792.1:c.3539A>T	NP_001369721.1:p.Glu1180Val
NM_001382793.1:c.3533A>T	NP_001369722.1:p.Glu1178Val
NM_001382794.1:c.3533A>T	NP_001369723.1:p.Glu1178Val
NM_001382795.1:c.3527A>T	NP_001369724.1:p.Glu1176Val
NM_001382796.1:c.3488A>T	NP_001369725.1:p.Glu1163Val
NM_001382797.1:c.3476A>T	NP_001369726.1:p.Glu1159Val
NM_001382798.1:c.3419A>T	NP_001369727.1:p.Glu1140Val
NM_001382799.1:c.3395A>T	NP_001369728.1:p.Glu1132Val
NM_001382800.1:c.3389A>T	NP_001369729.1:p.Glu1130Val
NM_001382801.1:c.3371A>T	NP_001369730.1:p.Glu1124Val
NM_001382802.1:c.3317A>T	NP_001369731.1:p.Glu1106Val
NM_001382803.1:c.*154A>T	NP_001369732.1:n.*154A>T
NM_001382804.1:c.2747A>T	NP_001369733.1:p.Glu916Val
NM_001382805.1:c.2624A>T	NP_001369734.1:p.Glu875Val
NM_001382806.1:c.2537A>T	NP_001369735.1:p.Glu846Val
NM_004448.4:c.3575A>T MANE Select	NP_004439.2:p.Glu1192Val
NR_110535.2:n.3813A>T