Canonical Allele Identifier: CA399314423

Gene: ERBB2

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3669G>T MANE Select	ENSP00000269571.4:p.Trp1223Cys
ENST00000269571.9:c.3669G>T	ENSP00000269571.4:p.Trp1223Cys
ENST00000406381.6:c.3579G>T	ENSP00000385185.2:p.Trp1193Cys
ENST00000445658.6:c.2841G>T	ENSP00000404047.2:p.Trp947Cys
ENST00000541774.5:c.3624G>T	ENSP00000446466.1:p.Trp1208Cys
ENST00000578373.5:c.*3459G>T	ENSP00000463427.1:n.*3459G>T
ENST00000584450.5:c.*248G>T	ENSP00000463714.1:n.*248G>T
ENST00000584601.5:c.3579G>T	ENSP00000462438.1:p.Trp1193Cys
NM_001005862.2:c.3579G>T , LRG_724t1:c.3579G>T	NP_001005862.1:p.Trp1193Cys
NM_001289936.1:c.3624G>T , LRG_724t4:c.3624G>T	NP_001276865.1:p.Trp1208Cys
NM_001289937.1:c.*248G>T	NP_001276866.1:n.*248G>T
NM_004448.3:c.3669G>T , LRG_724t2:c.3669G>T	NP_004439.2:p.Trp1223Cys
NR_110535.1:n.3993G>T
XM_024450641.1:c.3807G>T	XP_024306409.1:p.Trp1269Cys
XM_024450642.1:c.3762G>T	XP_024306410.1:p.Trp1254Cys
XM_024450643.1:c.3717G>T	XP_024306411.1:p.Trp1239Cys
NM_001005862.3:c.3579G>T	NP_001005862.1:p.Trp1193Cys
NM_001289936.2:c.3624G>T	NP_001276865.1:p.Trp1208Cys
NM_001289937.2:c.*248G>T	NP_001276866.1:n.*248G>T
NM_001382782.1:c.3579G>T	NP_001369711.1:p.Trp1193Cys
NM_001382783.1:c.3579G>T	NP_001369712.1:p.Trp1193Cys
NM_001382784.1:c.3786G>T	NP_001369713.1:p.Trp1262Cys
NM_001382785.1:c.3771G>T	NP_001369714.1:p.Trp1257Cys
NM_001382786.1:c.3750G>T	NP_001369715.1:p.Trp1250Cys
NM_001382787.1:c.3744G>T	NP_001369716.1:p.Trp1248Cys
NM_001382788.1:c.3699G>T	NP_001369717.1:p.Trp1233Cys
NM_001382789.1:c.3690G>T	NP_001369718.1:p.Trp1230Cys
NM_001382790.1:c.3666G>T	NP_001369719.1:p.Trp1222Cys
NM_001382791.1:c.3660G>T	NP_001369720.1:p.Trp1220Cys
NM_001382792.1:c.3633G>T	NP_001369721.1:p.Trp1211Cys
NM_001382793.1:c.3627G>T	NP_001369722.1:p.Trp1209Cys
NM_001382794.1:c.3627G>T	NP_001369723.1:p.Trp1209Cys
NM_001382795.1:c.3621G>T	NP_001369724.1:p.Trp1207Cys
NM_001382796.1:c.3582G>T	NP_001369725.1:p.Trp1194Cys
NM_001382797.1:c.3570G>T	NP_001369726.1:p.Trp1190Cys
NM_001382798.1:c.3513G>T	NP_001369727.1:p.Trp1171Cys
NM_001382799.1:c.3489G>T	NP_001369728.1:p.Trp1163Cys
NM_001382800.1:c.3483G>T	NP_001369729.1:p.Trp1161Cys
NM_001382801.1:c.3465G>T	NP_001369730.1:p.Trp1155Cys
NM_001382802.1:c.3411G>T	NP_001369731.1:p.Trp1137Cys
NM_001382803.1:c.*248G>T	NP_001369732.1:n.*248G>T
NM_001382804.1:c.2841G>T	NP_001369733.1:p.Trp947Cys
NM_001382805.1:c.2718G>T	NP_001369734.1:p.Trp906Cys
NM_001382806.1:c.2631G>T	NP_001369735.1:p.Trp877Cys
NM_004448.4:c.3669G>T MANE Select	NP_004439.2:p.Trp1223Cys
NR_110535.2:n.3907G>T