Canonical Allele Identifier: CA399310490

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143241411
• MyVariant Identifiers: chr17:g.37883633G>A (hg19) ; chr17:g.39727380G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727380G>A , CM000679.2:g.39727380G>A	GRCh38
NC_000017.10:g.37883633G>A , CM000679.1:g.37883633G>A	GRCh37
NC_000017.9:g.35137159G>A	NCBI36
NG_007503.1:g.44241G>A , LRG_724:g.44241G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3245G>A MANE Select	ENSP00000269571.4:p.Gly1082Asp
ENST00000269571.9:c.3245G>A	ENSP00000269571.4:p.Gly1082Asp
ENST00000406381.6:c.3155G>A	ENSP00000385185.2:p.Gly1052Asp
ENST00000445658.6:c.2417G>A	ENSP00000404047.2:p.Gly806Asp
ENST00000541774.5:c.3200G>A	ENSP00000446466.1:p.Gly1067Asp
ENST00000578373.5:c.*3035G>A	ENSP00000463427.1:n.*3035G>A
ENST00000584450.5:c.3160-309G>A	ENSP00000463714.1:n.3160-309G>A
ENST00000584601.5:c.3155G>A	ENSP00000462438.1:p.Gly1052Asp
NM_001005862.2:c.3155G>A , LRG_724t1:c.3155G>A	NP_001005862.1:p.Gly1052Asp
NM_001289936.1:c.3200G>A , LRG_724t4:c.3200G>A	NP_001276865.1:p.Gly1067Asp
NM_001289937.1:c.3160-309G>A	NP_001276866.1:n.3160-309G>A
NM_004448.3:c.3245G>A , LRG_724t2:c.3245G>A	NP_004439.2:p.Gly1082Asp
NR_110535.1:n.3569G>A
XM_024450641.1:c.3383G>A	XP_024306409.1:p.Gly1128Asp
XM_024450642.1:c.3338G>A	XP_024306410.1:p.Gly1113Asp
XM_024450643.1:c.3293G>A	XP_024306411.1:p.Gly1098Asp
NM_001005862.3:c.3155G>A	NP_001005862.1:p.Gly1052Asp
NM_001289936.2:c.3200G>A	NP_001276865.1:p.Gly1067Asp
NM_001289937.2:c.3160-309G>A	NP_001276866.1:n.3160-309G>A
NM_001382782.1:c.3155G>A	NP_001369711.1:p.Gly1052Asp
NM_001382783.1:c.3155G>A	NP_001369712.1:p.Gly1052Asp
NM_001382784.1:c.3362G>A	NP_001369713.1:p.Gly1121Asp
NM_001382785.1:c.3347G>A	NP_001369714.1:p.Gly1116Asp
NM_001382786.1:c.3326G>A	NP_001369715.1:p.Gly1109Asp
NM_001382787.1:c.3320G>A	NP_001369716.1:p.Gly1107Asp
NM_001382788.1:c.3275G>A	NP_001369717.1:p.Gly1092Asp
NM_001382789.1:c.3266G>A	NP_001369718.1:p.Gly1089Asp
NM_001382790.1:c.3242G>A	NP_001369719.1:p.Gly1081Asp
NM_001382791.1:c.3236G>A	NP_001369720.1:p.Gly1079Asp
NM_001382792.1:c.3209G>A	NP_001369721.1:p.Gly1070Asp
NM_001382793.1:c.3203G>A	NP_001369722.1:p.Gly1068Asp
NM_001382794.1:c.3203G>A	NP_001369723.1:p.Gly1068Asp
NM_001382795.1:c.3197G>A	NP_001369724.1:p.Gly1066Asp
NM_001382796.1:c.3158G>A	NP_001369725.1:p.Gly1053Asp
NM_001382797.1:c.3146G>A	NP_001369726.1:p.Gly1049Asp
NM_001382798.1:c.3089G>A	NP_001369727.1:p.Gly1030Asp
NM_001382799.1:c.3065G>A	NP_001369728.1:p.Gly1022Asp
NM_001382800.1:c.3059G>A	NP_001369729.1:p.Gly1020Asp
NM_001382801.1:c.3041G>A	NP_001369730.1:p.Gly1014Asp
NM_001382802.1:c.2987G>A	NP_001369731.1:p.Gly996Asp
NM_001382803.1:c.3118-309G>A	NP_001369732.1:n.3118-309G>A
NM_001382804.1:c.2417G>A	NP_001369733.1:p.Gly806Asp
NM_001382805.1:c.2294G>A	NP_001369734.1:p.Gly765Asp
NM_001382806.1:c.2207G>A	NP_001369735.1:p.Gly736Asp
NM_004448.4:c.3245G>A MANE Select	NP_004439.2:p.Gly1082Asp
NR_110535.2:n.3483G>A