Canonical Allele Identifier: CA399311000

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143249887
• MyVariant Identifiers: chr17:g.37883704C>A (hg19) ; chr17:g.39727451C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727451C>A , CM000679.2:g.39727451C>A	GRCh38
NC_000017.10:g.37883704C>A , CM000679.1:g.37883704C>A	GRCh37
NC_000017.9:g.35137230C>A	NCBI36
NG_007503.1:g.44312C>A , LRG_724:g.44312C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3316C>A MANE Select	ENSP00000269571.4:p.Pro1106Thr
ENST00000269571.9:c.3316C>A	ENSP00000269571.4:p.Pro1106Thr
ENST00000406381.6:c.3226C>A	ENSP00000385185.2:p.Pro1076Thr
ENST00000445658.6:c.2488C>A	ENSP00000404047.2:p.Pro830Thr
ENST00000541774.5:c.3271C>A	ENSP00000446466.1:p.Pro1091Thr
ENST00000578373.5:c.*3106C>A	ENSP00000463427.1:n.*3106C>A
ENST00000584450.5:c.3160-238C>A	ENSP00000463714.1:n.3160-238C>A
ENST00000584601.5:c.3226C>A	ENSP00000462438.1:p.Pro1076Thr
NM_001005862.2:c.3226C>A , LRG_724t1:c.3226C>A	NP_001005862.1:p.Pro1076Thr
NM_001289936.1:c.3271C>A , LRG_724t4:c.3271C>A	NP_001276865.1:p.Pro1091Thr
NM_001289937.1:c.3160-238C>A	NP_001276866.1:n.3160-238C>A
NM_004448.3:c.3316C>A , LRG_724t2:c.3316C>A	NP_004439.2:p.Pro1106Thr
NR_110535.1:n.3640C>A
XM_024450641.1:c.3454C>A	XP_024306409.1:p.Pro1152Thr
XM_024450642.1:c.3409C>A	XP_024306410.1:p.Pro1137Thr
XM_024450643.1:c.3364C>A	XP_024306411.1:p.Pro1122Thr
NM_001005862.3:c.3226C>A	NP_001005862.1:p.Pro1076Thr
NM_001289936.2:c.3271C>A	NP_001276865.1:p.Pro1091Thr
NM_001289937.2:c.3160-238C>A	NP_001276866.1:n.3160-238C>A
NM_001382782.1:c.3226C>A	NP_001369711.1:p.Pro1076Thr
NM_001382783.1:c.3226C>A	NP_001369712.1:p.Pro1076Thr
NM_001382784.1:c.3433C>A	NP_001369713.1:p.Pro1145Thr
NM_001382785.1:c.3418C>A	NP_001369714.1:p.Pro1140Thr
NM_001382786.1:c.3397C>A	NP_001369715.1:p.Pro1133Thr
NM_001382787.1:c.3391C>A	NP_001369716.1:p.Pro1131Thr
NM_001382788.1:c.3346C>A	NP_001369717.1:p.Pro1116Thr
NM_001382789.1:c.3337C>A	NP_001369718.1:p.Pro1113Thr
NM_001382790.1:c.3313C>A	NP_001369719.1:p.Pro1105Thr
NM_001382791.1:c.3307C>A	NP_001369720.1:p.Pro1103Thr
NM_001382792.1:c.3280C>A	NP_001369721.1:p.Pro1094Thr
NM_001382793.1:c.3274C>A	NP_001369722.1:p.Pro1092Thr
NM_001382794.1:c.3274C>A	NP_001369723.1:p.Pro1092Thr
NM_001382795.1:c.3268C>A	NP_001369724.1:p.Pro1090Thr
NM_001382796.1:c.3229C>A	NP_001369725.1:p.Pro1077Thr
NM_001382797.1:c.3217C>A	NP_001369726.1:p.Pro1073Thr
NM_001382798.1:c.3160C>A	NP_001369727.1:p.Pro1054Thr
NM_001382799.1:c.3136C>A	NP_001369728.1:p.Pro1046Thr
NM_001382800.1:c.3130C>A	NP_001369729.1:p.Pro1044Thr
NM_001382801.1:c.3112C>A	NP_001369730.1:p.Pro1038Thr
NM_001382802.1:c.3058C>A	NP_001369731.1:p.Pro1020Thr
NM_001382803.1:c.3118-238C>A	NP_001369732.1:n.3118-238C>A
NM_001382804.1:c.2488C>A	NP_001369733.1:p.Pro830Thr
NM_001382805.1:c.2365C>A	NP_001369734.1:p.Pro789Thr
NM_001382806.1:c.2278C>A	NP_001369735.1:p.Pro760Thr
NM_004448.4:c.3316C>A MANE Select	NP_004439.2:p.Pro1106Thr
NR_110535.2:n.3554C>A