Canonical Allele Identifier: CA399312746

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143257892
• MyVariant Identifiers: chr17:g.37883771T>G (hg19) ; chr17:g.39727518T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727518T>G , CM000679.2:g.39727518T>G	GRCh38
NC_000017.10:g.37883771T>G , CM000679.1:g.37883771T>G	GRCh37
NC_000017.9:g.35137297T>G	NCBI36
NG_007503.1:g.44379T>G , LRG_724:g.44379T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3383T>G MANE Select	ENSP00000269571.4:p.Val1128Gly
ENST00000269571.9:c.3383T>G	ENSP00000269571.4:p.Val1128Gly
ENST00000406381.6:c.3293T>G	ENSP00000385185.2:p.Val1098Gly
ENST00000445658.6:c.2555T>G	ENSP00000404047.2:p.Val852Gly
ENST00000541774.5:c.3338T>G	ENSP00000446466.1:p.Val1113Gly
ENST00000578373.5:c.*3173T>G	ENSP00000463427.1:n.*3173T>G
ENST00000584450.5:c.3160-171T>G	ENSP00000463714.1:n.3160-171T>G
ENST00000584601.5:c.3293T>G	ENSP00000462438.1:p.Val1098Gly
NM_001005862.2:c.3293T>G , LRG_724t1:c.3293T>G	NP_001005862.1:p.Val1098Gly
NM_001289936.1:c.3338T>G , LRG_724t4:c.3338T>G	NP_001276865.1:p.Val1113Gly
NM_001289937.1:c.3160-171T>G	NP_001276866.1:n.3160-171T>G
NM_004448.3:c.3383T>G , LRG_724t2:c.3383T>G	NP_004439.2:p.Val1128Gly
NR_110535.1:n.3707T>G
XM_024450641.1:c.3521T>G	XP_024306409.1:p.Val1174Gly
XM_024450642.1:c.3476T>G	XP_024306410.1:p.Val1159Gly
XM_024450643.1:c.3431T>G	XP_024306411.1:p.Val1144Gly
NM_001005862.3:c.3293T>G	NP_001005862.1:p.Val1098Gly
NM_001289936.2:c.3338T>G	NP_001276865.1:p.Val1113Gly
NM_001289937.2:c.3160-171T>G	NP_001276866.1:n.3160-171T>G
NM_001382782.1:c.3293T>G	NP_001369711.1:p.Val1098Gly
NM_001382783.1:c.3293T>G	NP_001369712.1:p.Val1098Gly
NM_001382784.1:c.3500T>G	NP_001369713.1:p.Val1167Gly
NM_001382785.1:c.3485T>G	NP_001369714.1:p.Val1162Gly
NM_001382786.1:c.3464T>G	NP_001369715.1:p.Val1155Gly
NM_001382787.1:c.3458T>G	NP_001369716.1:p.Val1153Gly
NM_001382788.1:c.3413T>G	NP_001369717.1:p.Val1138Gly
NM_001382789.1:c.3404T>G	NP_001369718.1:p.Val1135Gly
NM_001382790.1:c.3380T>G	NP_001369719.1:p.Val1127Gly
NM_001382791.1:c.3374T>G	NP_001369720.1:p.Val1125Gly
NM_001382792.1:c.3347T>G	NP_001369721.1:p.Val1116Gly
NM_001382793.1:c.3341T>G	NP_001369722.1:p.Val1114Gly
NM_001382794.1:c.3341T>G	NP_001369723.1:p.Val1114Gly
NM_001382795.1:c.3335T>G	NP_001369724.1:p.Val1112Gly
NM_001382796.1:c.3296T>G	NP_001369725.1:p.Val1099Gly
NM_001382797.1:c.3284T>G	NP_001369726.1:p.Val1095Gly
NM_001382798.1:c.3227T>G	NP_001369727.1:p.Val1076Gly
NM_001382799.1:c.3203T>G	NP_001369728.1:p.Val1068Gly
NM_001382800.1:c.3197T>G	NP_001369729.1:p.Val1066Gly
NM_001382801.1:c.3179T>G	NP_001369730.1:p.Val1060Gly
NM_001382802.1:c.3125T>G	NP_001369731.1:p.Val1042Gly
NM_001382803.1:c.3118-171T>G	NP_001369732.1:n.3118-171T>G
NM_001382804.1:c.2555T>G	NP_001369733.1:p.Val852Gly
NM_001382805.1:c.2432T>G	NP_001369734.1:p.Val811Gly
NM_001382806.1:c.2345T>G	NP_001369735.1:p.Val782Gly
NM_004448.4:c.3383T>G MANE Select	NP_004439.2:p.Val1128Gly
NR_110535.2:n.3621T>G