Canonical Allele Identifier: CA399314417

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143313479
• MyVariant Identifiers: chr17:g.37884198G>A (hg19) ; chr17:g.39727945G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727945G>A , CM000679.2:g.39727945G>A	GRCh38
NC_000017.10:g.37884198G>A , CM000679.1:g.37884198G>A	GRCh37
NC_000017.9:g.35137724G>A	NCBI36
NG_007503.1:g.44806G>A , LRG_724:g.44806G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3669G>A MANE Select	ENSP00000269571.4:p.Trp1223Ter
ENST00000269571.9:c.3669G>A	ENSP00000269571.4:p.Trp1223Ter
ENST00000406381.6:c.3579G>A	ENSP00000385185.2:p.Trp1193Ter
ENST00000445658.6:c.2841G>A	ENSP00000404047.2:p.Trp947Ter
ENST00000541774.5:c.3624G>A	ENSP00000446466.1:p.Trp1208Ter
ENST00000578373.5:c.*3459G>A	ENSP00000463427.1:n.*3459G>A
ENST00000584450.5:c.*248G>A	ENSP00000463714.1:n.*248G>A
ENST00000584601.5:c.3579G>A	ENSP00000462438.1:p.Trp1193Ter
NM_001005862.2:c.3579G>A , LRG_724t1:c.3579G>A	NP_001005862.1:p.Trp1193Ter
NM_001289936.1:c.3624G>A , LRG_724t4:c.3624G>A	NP_001276865.1:p.Trp1208Ter
NM_001289937.1:c.*248G>A	NP_001276866.1:n.*248G>A
NM_004448.3:c.3669G>A , LRG_724t2:c.3669G>A	NP_004439.2:p.Trp1223Ter
NR_110535.1:n.3993G>A
XM_024450641.1:c.3807G>A	XP_024306409.1:p.Trp1269Ter
XM_024450642.1:c.3762G>A	XP_024306410.1:p.Trp1254Ter
XM_024450643.1:c.3717G>A	XP_024306411.1:p.Trp1239Ter
NM_001005862.3:c.3579G>A	NP_001005862.1:p.Trp1193Ter
NM_001289936.2:c.3624G>A	NP_001276865.1:p.Trp1208Ter
NM_001289937.2:c.*248G>A	NP_001276866.1:n.*248G>A
NM_001382782.1:c.3579G>A	NP_001369711.1:p.Trp1193Ter
NM_001382783.1:c.3579G>A	NP_001369712.1:p.Trp1193Ter
NM_001382784.1:c.3786G>A	NP_001369713.1:p.Trp1262Ter
NM_001382785.1:c.3771G>A	NP_001369714.1:p.Trp1257Ter
NM_001382786.1:c.3750G>A	NP_001369715.1:p.Trp1250Ter
NM_001382787.1:c.3744G>A	NP_001369716.1:p.Trp1248Ter
NM_001382788.1:c.3699G>A	NP_001369717.1:p.Trp1233Ter
NM_001382789.1:c.3690G>A	NP_001369718.1:p.Trp1230Ter
NM_001382790.1:c.3666G>A	NP_001369719.1:p.Trp1222Ter
NM_001382791.1:c.3660G>A	NP_001369720.1:p.Trp1220Ter
NM_001382792.1:c.3633G>A	NP_001369721.1:p.Trp1211Ter
NM_001382793.1:c.3627G>A	NP_001369722.1:p.Trp1209Ter
NM_001382794.1:c.3627G>A	NP_001369723.1:p.Trp1209Ter
NM_001382795.1:c.3621G>A	NP_001369724.1:p.Trp1207Ter
NM_001382796.1:c.3582G>A	NP_001369725.1:p.Trp1194Ter
NM_001382797.1:c.3570G>A	NP_001369726.1:p.Trp1190Ter
NM_001382798.1:c.3513G>A	NP_001369727.1:p.Trp1171Ter
NM_001382799.1:c.3489G>A	NP_001369728.1:p.Trp1163Ter
NM_001382800.1:c.3483G>A	NP_001369729.1:p.Trp1161Ter
NM_001382801.1:c.3465G>A	NP_001369730.1:p.Trp1155Ter
NM_001382802.1:c.3411G>A	NP_001369731.1:p.Trp1137Ter
NM_001382803.1:c.*248G>A	NP_001369732.1:n.*248G>A
NM_001382804.1:c.2841G>A	NP_001369733.1:p.Trp947Ter
NM_001382805.1:c.2718G>A	NP_001369734.1:p.Trp906Ter
NM_001382806.1:c.2631G>A	NP_001369735.1:p.Trp877Ter
NM_004448.4:c.3669G>A MANE Select	NP_004439.2:p.Trp1223Ter
NR_110535.2:n.3907G>A