Canonical Allele Identifier: CA399313166

Gene: ERBB2

Linked Data

• dbSNP Id: rs1423726828
• gnomAD v4: 17-39727778-G-T
• MyVariant Identifiers: chr17:g.37884031G>T (hg19) ; chr17:g.39727778G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727778G>T , CM000679.2:g.39727778G>T	GRCh38
NC_000017.10:g.37884031G>T , CM000679.1:g.37884031G>T	GRCh37
NC_000017.9:g.35137557G>T	NCBI36
NG_007503.1:g.44639G>T , LRG_724:g.44639G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3502G>T MANE Select	ENSP00000269571.4:p.Glu1168Ter
ENST00000269571.9:c.3502G>T	ENSP00000269571.4:p.Glu1168Ter
ENST00000406381.6:c.3412G>T	ENSP00000385185.2:p.Glu1138Ter
ENST00000445658.6:c.2674G>T	ENSP00000404047.2:p.Glu892Ter
ENST00000541774.5:c.3457G>T	ENSP00000446466.1:p.Glu1153Ter
ENST00000578373.5:c.*3292G>T	ENSP00000463427.1:n.*3292G>T
ENST00000584450.5:c.*81G>T	ENSP00000463714.1:n.*81G>T
ENST00000584601.5:c.3412G>T	ENSP00000462438.1:p.Glu1138Ter
NM_001005862.2:c.3412G>T , LRG_724t1:c.3412G>T	NP_001005862.1:p.Glu1138Ter
NM_001289936.1:c.3457G>T , LRG_724t4:c.3457G>T	NP_001276865.1:p.Glu1153Ter
NM_001289937.1:c.*81G>T	NP_001276866.1:n.*81G>T
NM_004448.3:c.3502G>T , LRG_724t2:c.3502G>T	NP_004439.2:p.Glu1168Ter
NR_110535.1:n.3826G>T
XM_024450641.1:c.3640G>T	XP_024306409.1:p.Glu1214Ter
XM_024450642.1:c.3595G>T	XP_024306410.1:p.Glu1199Ter
XM_024450643.1:c.3550G>T	XP_024306411.1:p.Glu1184Ter
NM_001005862.3:c.3412G>T	NP_001005862.1:p.Glu1138Ter
NM_001289936.2:c.3457G>T	NP_001276865.1:p.Glu1153Ter
NM_001289937.2:c.*81G>T	NP_001276866.1:n.*81G>T
NM_001382782.1:c.3412G>T	NP_001369711.1:p.Glu1138Ter
NM_001382783.1:c.3412G>T	NP_001369712.1:p.Glu1138Ter
NM_001382784.1:c.3619G>T	NP_001369713.1:p.Glu1207Ter
NM_001382785.1:c.3604G>T	NP_001369714.1:p.Glu1202Ter
NM_001382786.1:c.3583G>T	NP_001369715.1:p.Glu1195Ter
NM_001382787.1:c.3577G>T	NP_001369716.1:p.Glu1193Ter
NM_001382788.1:c.3532G>T	NP_001369717.1:p.Glu1178Ter
NM_001382789.1:c.3523G>T	NP_001369718.1:p.Glu1175Ter
NM_001382790.1:c.3499G>T	NP_001369719.1:p.Glu1167Ter
NM_001382791.1:c.3493G>T	NP_001369720.1:p.Glu1165Ter
NM_001382792.1:c.3466G>T	NP_001369721.1:p.Glu1156Ter
NM_001382793.1:c.3460G>T	NP_001369722.1:p.Glu1154Ter
NM_001382794.1:c.3460G>T	NP_001369723.1:p.Glu1154Ter
NM_001382795.1:c.3454G>T	NP_001369724.1:p.Glu1152Ter
NM_001382796.1:c.3415G>T	NP_001369725.1:p.Glu1139Ter
NM_001382797.1:c.3403G>T	NP_001369726.1:p.Glu1135Ter
NM_001382798.1:c.3346G>T	NP_001369727.1:p.Glu1116Ter
NM_001382799.1:c.3322G>T	NP_001369728.1:p.Glu1108Ter
NM_001382800.1:c.3316G>T	NP_001369729.1:p.Glu1106Ter
NM_001382801.1:c.3298G>T	NP_001369730.1:p.Glu1100Ter
NM_001382802.1:c.3244G>T	NP_001369731.1:p.Glu1082Ter
NM_001382803.1:c.*81G>T	NP_001369732.1:n.*81G>T
NM_001382804.1:c.2674G>T	NP_001369733.1:p.Glu892Ter
NM_001382805.1:c.2551G>T	NP_001369734.1:p.Glu851Ter
NM_001382806.1:c.2464G>T	NP_001369735.1:p.Glu822Ter
NM_004448.4:c.3502G>T MANE Select	NP_004439.2:p.Glu1168Ter
NR_110535.2:n.3740G>T