Canonical Allele Identifier: CA399312863

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143288366
• MyVariant Identifiers: chr17:g.37883962G>T (hg19) ; chr17:g.39727709G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727709G>T , CM000679.2:g.39727709G>T	GRCh38
NC_000017.10:g.37883962G>T , CM000679.1:g.37883962G>T	GRCh37
NC_000017.9:g.35137488G>T	NCBI36
NG_007503.1:g.44570G>T , LRG_724:g.44570G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3433G>T MANE Select	ENSP00000269571.4:p.Val1145Phe
ENST00000269571.9:c.3433G>T	ENSP00000269571.4:p.Val1145Phe
ENST00000406381.6:c.3343G>T	ENSP00000385185.2:p.Val1115Phe
ENST00000445658.6:c.2605G>T	ENSP00000404047.2:p.Val869Phe
ENST00000541774.5:c.3388G>T	ENSP00000446466.1:p.Val1130Phe
ENST00000578373.5:c.*3223G>T	ENSP00000463427.1:n.*3223G>T
ENST00000584450.5:c.*12G>T	ENSP00000463714.1:n.*12G>T
ENST00000584601.5:c.3343G>T	ENSP00000462438.1:p.Val1115Phe
NM_001005862.2:c.3343G>T , LRG_724t1:c.3343G>T	NP_001005862.1:p.Val1115Phe
NM_001289936.1:c.3388G>T , LRG_724t4:c.3388G>T	NP_001276865.1:p.Val1130Phe
NM_001289937.1:c.*12G>T	NP_001276866.1:n.*12G>T
NM_004448.3:c.3433G>T , LRG_724t2:c.3433G>T	NP_004439.2:p.Val1145Phe
NR_110535.1:n.3757G>T
XM_024450641.1:c.3571G>T	XP_024306409.1:p.Val1191Phe
XM_024450642.1:c.3526G>T	XP_024306410.1:p.Val1176Phe
XM_024450643.1:c.3481G>T	XP_024306411.1:p.Val1161Phe
NM_001005862.3:c.3343G>T	NP_001005862.1:p.Val1115Phe
NM_001289936.2:c.3388G>T	NP_001276865.1:p.Val1130Phe
NM_001289937.2:c.*12G>T	NP_001276866.1:n.*12G>T
NM_001382782.1:c.3343G>T	NP_001369711.1:p.Val1115Phe
NM_001382783.1:c.3343G>T	NP_001369712.1:p.Val1115Phe
NM_001382784.1:c.3550G>T	NP_001369713.1:p.Val1184Phe
NM_001382785.1:c.3535G>T	NP_001369714.1:p.Val1179Phe
NM_001382786.1:c.3514G>T	NP_001369715.1:p.Val1172Phe
NM_001382787.1:c.3508G>T	NP_001369716.1:p.Val1170Phe
NM_001382788.1:c.3463G>T	NP_001369717.1:p.Val1155Phe
NM_001382789.1:c.3454G>T	NP_001369718.1:p.Val1152Phe
NM_001382790.1:c.3430G>T	NP_001369719.1:p.Val1144Phe
NM_001382791.1:c.3424G>T	NP_001369720.1:p.Val1142Phe
NM_001382792.1:c.3397G>T	NP_001369721.1:p.Val1133Phe
NM_001382793.1:c.3391G>T	NP_001369722.1:p.Val1131Phe
NM_001382794.1:c.3391G>T	NP_001369723.1:p.Val1131Phe
NM_001382795.1:c.3385G>T	NP_001369724.1:p.Val1129Phe
NM_001382796.1:c.3346G>T	NP_001369725.1:p.Val1116Phe
NM_001382797.1:c.3334G>T	NP_001369726.1:p.Val1112Phe
NM_001382798.1:c.3277G>T	NP_001369727.1:p.Val1093Phe
NM_001382799.1:c.3253G>T	NP_001369728.1:p.Val1085Phe
NM_001382800.1:c.3247G>T	NP_001369729.1:p.Val1083Phe
NM_001382801.1:c.3229G>T	NP_001369730.1:p.Val1077Phe
NM_001382802.1:c.3175G>T	NP_001369731.1:p.Val1059Phe
NM_001382803.1:c.*12G>T	NP_001369732.1:n.*12G>T
NM_001382804.1:c.2605G>T	NP_001369733.1:p.Val869Phe
NM_001382805.1:c.2482G>T	NP_001369734.1:p.Val828Phe
NM_001382806.1:c.2395G>T	NP_001369735.1:p.Val799Phe
NM_004448.4:c.3433G>T MANE Select	NP_004439.2:p.Val1145Phe
NR_110535.2:n.3671G>T