Canonical Allele Identifier: CA399310660

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143244498
• gnomAD v4: 17-39727406-G-T
• MyVariant Identifiers: chr17:g.37883659G>T (hg19) ; chr17:g.39727406G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727406G>T , CM000679.2:g.39727406G>T	GRCh38
NC_000017.10:g.37883659G>T , CM000679.1:g.37883659G>T	GRCh37
NC_000017.9:g.35137185G>T	NCBI36
NG_007503.1:g.44267G>T , LRG_724:g.44267G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3271G>T MANE Select	ENSP00000269571.4:p.Gly1091Ter
ENST00000269571.9:c.3271G>T	ENSP00000269571.4:p.Gly1091Ter
ENST00000406381.6:c.3181G>T	ENSP00000385185.2:p.Gly1061Ter
ENST00000445658.6:c.2443G>T	ENSP00000404047.2:p.Gly815Ter
ENST00000541774.5:c.3226G>T	ENSP00000446466.1:p.Gly1076Ter
ENST00000578373.5:c.*3061G>T	ENSP00000463427.1:n.*3061G>T
ENST00000584450.5:c.3160-283G>T	ENSP00000463714.1:n.3160-283G>T
ENST00000584601.5:c.3181G>T	ENSP00000462438.1:p.Gly1061Ter
NM_001005862.2:c.3181G>T , LRG_724t1:c.3181G>T	NP_001005862.1:p.Gly1061Ter
NM_001289936.1:c.3226G>T , LRG_724t4:c.3226G>T	NP_001276865.1:p.Gly1076Ter
NM_001289937.1:c.3160-283G>T	NP_001276866.1:n.3160-283G>T
NM_004448.3:c.3271G>T , LRG_724t2:c.3271G>T	NP_004439.2:p.Gly1091Ter
NR_110535.1:n.3595G>T
XM_024450641.1:c.3409G>T	XP_024306409.1:p.Gly1137Ter
XM_024450642.1:c.3364G>T	XP_024306410.1:p.Gly1122Ter
XM_024450643.1:c.3319G>T	XP_024306411.1:p.Gly1107Ter
NM_001005862.3:c.3181G>T	NP_001005862.1:p.Gly1061Ter
NM_001289936.2:c.3226G>T	NP_001276865.1:p.Gly1076Ter
NM_001289937.2:c.3160-283G>T	NP_001276866.1:n.3160-283G>T
NM_001382782.1:c.3181G>T	NP_001369711.1:p.Gly1061Ter
NM_001382783.1:c.3181G>T	NP_001369712.1:p.Gly1061Ter
NM_001382784.1:c.3388G>T	NP_001369713.1:p.Gly1130Ter
NM_001382785.1:c.3373G>T	NP_001369714.1:p.Gly1125Ter
NM_001382786.1:c.3352G>T	NP_001369715.1:p.Gly1118Ter
NM_001382787.1:c.3346G>T	NP_001369716.1:p.Gly1116Ter
NM_001382788.1:c.3301G>T	NP_001369717.1:p.Gly1101Ter
NM_001382789.1:c.3292G>T	NP_001369718.1:p.Gly1098Ter
NM_001382790.1:c.3268G>T	NP_001369719.1:p.Gly1090Ter
NM_001382791.1:c.3262G>T	NP_001369720.1:p.Gly1088Ter
NM_001382792.1:c.3235G>T	NP_001369721.1:p.Gly1079Ter
NM_001382793.1:c.3229G>T	NP_001369722.1:p.Gly1077Ter
NM_001382794.1:c.3229G>T	NP_001369723.1:p.Gly1077Ter
NM_001382795.1:c.3223G>T	NP_001369724.1:p.Gly1075Ter
NM_001382796.1:c.3184G>T	NP_001369725.1:p.Gly1062Ter
NM_001382797.1:c.3172G>T	NP_001369726.1:p.Gly1058Ter
NM_001382798.1:c.3115G>T	NP_001369727.1:p.Gly1039Ter
NM_001382799.1:c.3091G>T	NP_001369728.1:p.Gly1031Ter
NM_001382800.1:c.3085G>T	NP_001369729.1:p.Gly1029Ter
NM_001382801.1:c.3067G>T	NP_001369730.1:p.Gly1023Ter
NM_001382802.1:c.3013G>T	NP_001369731.1:p.Gly1005Ter
NM_001382803.1:c.3118-283G>T	NP_001369732.1:n.3118-283G>T
NM_001382804.1:c.2443G>T	NP_001369733.1:p.Gly815Ter
NM_001382805.1:c.2320G>T	NP_001369734.1:p.Gly774Ter
NM_001382806.1:c.2233G>T	NP_001369735.1:p.Gly745Ter
NM_004448.4:c.3271G>T MANE Select	NP_004439.2:p.Gly1091Ter
NR_110535.2:n.3509G>T