Canonical Allele Identifier: CA399310676

Gene: ERBB2

Linked Data

• dbSNP Id: rs771588633
• MyVariant Identifiers: chr17:g.37883666G>T (hg19) ; chr17:g.39727413G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727413G>T , CM000679.2:g.39727413G>T	GRCh38
NC_000017.10:g.37883666G>T , CM000679.1:g.37883666G>T	GRCh37
NC_000017.9:g.35137192G>T	NCBI36
NG_007503.1:g.44274G>T , LRG_724:g.44274G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3278G>T MANE Select	ENSP00000269571.4:p.Gly1093Val
ENST00000269571.9:c.3278G>T	ENSP00000269571.4:p.Gly1093Val
ENST00000406381.6:c.3188G>T	ENSP00000385185.2:p.Gly1063Val
ENST00000445658.6:c.2450G>T	ENSP00000404047.2:p.Gly817Val
ENST00000541774.5:c.3233G>T	ENSP00000446466.1:p.Gly1078Val
ENST00000578373.5:c.*3068G>T	ENSP00000463427.1:n.*3068G>T
ENST00000584450.5:c.3160-276G>T	ENSP00000463714.1:n.3160-276G>T
ENST00000584601.5:c.3188G>T	ENSP00000462438.1:p.Gly1063Val
NM_001005862.2:c.3188G>T , LRG_724t1:c.3188G>T	NP_001005862.1:p.Gly1063Val
NM_001289936.1:c.3233G>T , LRG_724t4:c.3233G>T	NP_001276865.1:p.Gly1078Val
NM_001289937.1:c.3160-276G>T	NP_001276866.1:n.3160-276G>T
NM_004448.3:c.3278G>T , LRG_724t2:c.3278G>T	NP_004439.2:p.Gly1093Val
NR_110535.1:n.3602G>T
XM_024450641.1:c.3416G>T	XP_024306409.1:p.Gly1139Val
XM_024450642.1:c.3371G>T	XP_024306410.1:p.Gly1124Val
XM_024450643.1:c.3326G>T	XP_024306411.1:p.Gly1109Val
NM_001005862.3:c.3188G>T	NP_001005862.1:p.Gly1063Val
NM_001289936.2:c.3233G>T	NP_001276865.1:p.Gly1078Val
NM_001289937.2:c.3160-276G>T	NP_001276866.1:n.3160-276G>T
NM_001382782.1:c.3188G>T	NP_001369711.1:p.Gly1063Val
NM_001382783.1:c.3188G>T	NP_001369712.1:p.Gly1063Val
NM_001382784.1:c.3395G>T	NP_001369713.1:p.Gly1132Val
NM_001382785.1:c.3380G>T	NP_001369714.1:p.Gly1127Val
NM_001382786.1:c.3359G>T	NP_001369715.1:p.Gly1120Val
NM_001382787.1:c.3353G>T	NP_001369716.1:p.Gly1118Val
NM_001382788.1:c.3308G>T	NP_001369717.1:p.Gly1103Val
NM_001382789.1:c.3299G>T	NP_001369718.1:p.Gly1100Val
NM_001382790.1:c.3275G>T	NP_001369719.1:p.Gly1092Val
NM_001382791.1:c.3269G>T	NP_001369720.1:p.Gly1090Val
NM_001382792.1:c.3242G>T	NP_001369721.1:p.Gly1081Val
NM_001382793.1:c.3236G>T	NP_001369722.1:p.Gly1079Val
NM_001382794.1:c.3236G>T	NP_001369723.1:p.Gly1079Val
NM_001382795.1:c.3230G>T	NP_001369724.1:p.Gly1077Val
NM_001382796.1:c.3191G>T	NP_001369725.1:p.Gly1064Val
NM_001382797.1:c.3179G>T	NP_001369726.1:p.Gly1060Val
NM_001382798.1:c.3122G>T	NP_001369727.1:p.Gly1041Val
NM_001382799.1:c.3098G>T	NP_001369728.1:p.Gly1033Val
NM_001382800.1:c.3092G>T	NP_001369729.1:p.Gly1031Val
NM_001382801.1:c.3074G>T	NP_001369730.1:p.Gly1025Val
NM_001382802.1:c.3020G>T	NP_001369731.1:p.Gly1007Val
NM_001382803.1:c.3118-276G>T	NP_001369732.1:n.3118-276G>T
NM_001382804.1:c.2450G>T	NP_001369733.1:p.Gly817Val
NM_001382805.1:c.2327G>T	NP_001369734.1:p.Gly776Val
NM_001382806.1:c.2240G>T	NP_001369735.1:p.Gly747Val
NM_004448.4:c.3278G>T MANE Select	NP_004439.2:p.Gly1093Val
NR_110535.2:n.3516G>T