Canonical Allele Identifier: CA499890291

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143259272
• MyVariant Identifiers: chr17:g.37883779C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727526C>T , CM000679.2:g.39727526C>T	GRCh38
NC_000017.10:g.37883779C>T , CM000679.1:g.37883779C>T	GRCh37
NC_000017.9:g.35137305C>T	NCBI36
NG_007503.1:g.44387C>T , LRG_724:g.44387C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3391C>T MANE Select	ENSP00000269571.4:p.Leu1131=
ENST00000269571.9:c.3391C>T	ENSP00000269571.4:p.Leu1131=
ENST00000406381.6:c.3301C>T	ENSP00000385185.2:p.Leu1101=
ENST00000445658.6:c.2563C>T	ENSP00000404047.2:p.Leu855=
ENST00000541774.5:c.3346C>T	ENSP00000446466.1:p.Leu1116=
ENST00000578373.5:c.*3181C>T	ENSP00000463427.1:n.*3181C>T
ENST00000584450.5:c.3160-163C>T	ENSP00000463714.1:n.3160-163C>T
ENST00000584601.5:c.3301C>T	ENSP00000462438.1:p.Leu1101=
NM_001005862.2:c.3301C>T , LRG_724t1:c.3301C>T	NP_001005862.1:p.Leu1101=
NM_001289936.1:c.3346C>T , LRG_724t4:c.3346C>T	NP_001276865.1:p.Leu1116=
NM_001289937.1:c.3160-163C>T	NP_001276866.1:n.3160-163C>T
NM_004448.3:c.3391C>T , LRG_724t2:c.3391C>T	NP_004439.2:p.Leu1131=
NR_110535.1:n.3715C>T
XM_024450641.1:c.3529C>T	XP_024306409.1:p.Leu1177=
XM_024450642.1:c.3484C>T	XP_024306410.1:p.Leu1162=
XM_024450643.1:c.3439C>T	XP_024306411.1:p.Leu1147=
NM_001005862.3:c.3301C>T	NP_001005862.1:p.Leu1101=
NM_001289936.2:c.3346C>T	NP_001276865.1:p.Leu1116=
NM_001289937.2:c.3160-163C>T	NP_001276866.1:n.3160-163C>T
NM_001382782.1:c.3301C>T	NP_001369711.1:p.Leu1101=
NM_001382783.1:c.3301C>T	NP_001369712.1:p.Leu1101=
NM_001382784.1:c.3508C>T	NP_001369713.1:p.Leu1170=
NM_001382785.1:c.3493C>T	NP_001369714.1:p.Leu1165=
NM_001382786.1:c.3472C>T	NP_001369715.1:p.Leu1158=
NM_001382787.1:c.3466C>T	NP_001369716.1:p.Leu1156=
NM_001382788.1:c.3421C>T	NP_001369717.1:p.Leu1141=
NM_001382789.1:c.3412C>T	NP_001369718.1:p.Leu1138=
NM_001382790.1:c.3388C>T	NP_001369719.1:p.Leu1130=
NM_001382791.1:c.3382C>T	NP_001369720.1:p.Leu1128=
NM_001382792.1:c.3355C>T	NP_001369721.1:p.Leu1119=
NM_001382793.1:c.3349C>T	NP_001369722.1:p.Leu1117=
NM_001382794.1:c.3349C>T	NP_001369723.1:p.Leu1117=
NM_001382795.1:c.3343C>T	NP_001369724.1:p.Leu1115=
NM_001382796.1:c.3304C>T	NP_001369725.1:p.Leu1102=
NM_001382797.1:c.3292C>T	NP_001369726.1:p.Leu1098=
NM_001382798.1:c.3235C>T	NP_001369727.1:p.Leu1079=
NM_001382799.1:c.3211C>T	NP_001369728.1:p.Leu1071=
NM_001382800.1:c.3205C>T	NP_001369729.1:p.Leu1069=
NM_001382801.1:c.3187C>T	NP_001369730.1:p.Leu1063=
NM_001382802.1:c.3133C>T	NP_001369731.1:p.Leu1045=
NM_001382803.1:c.3118-163C>T	NP_001369732.1:n.3118-163C>T
NM_001382804.1:c.2563C>T	NP_001369733.1:p.Leu855=
NM_001382805.1:c.2440C>T	NP_001369734.1:p.Leu814=
NM_001382806.1:c.2353C>T	NP_001369735.1:p.Leu785=
NM_004448.4:c.3391C>T MANE Select	NP_004439.2:p.Leu1131=
NR_110535.2:n.3629C>T