Canonical Allele Identifier: CA399312713

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143256444
• MyVariant Identifiers: chr17:g.37883762A>T (hg19) ; chr17:g.39727509A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727509A>T , CM000679.2:g.39727509A>T	GRCh38
NC_000017.10:g.37883762A>T , CM000679.1:g.37883762A>T	GRCh37
NC_000017.9:g.35137288A>T	NCBI36
NG_007503.1:g.44370A>T , LRG_724:g.44370A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3374A>T MANE Select	ENSP00000269571.4:p.Asp1125Val
ENST00000269571.9:c.3374A>T	ENSP00000269571.4:p.Asp1125Val
ENST00000406381.6:c.3284A>T	ENSP00000385185.2:p.Asp1095Val
ENST00000445658.6:c.2546A>T	ENSP00000404047.2:p.Asp849Val
ENST00000541774.5:c.3329A>T	ENSP00000446466.1:p.Asp1110Val
ENST00000578373.5:c.*3164A>T	ENSP00000463427.1:n.*3164A>T
ENST00000584450.5:c.3160-180A>T	ENSP00000463714.1:n.3160-180A>T
ENST00000584601.5:c.3284A>T	ENSP00000462438.1:p.Asp1095Val
NM_001005862.2:c.3284A>T , LRG_724t1:c.3284A>T	NP_001005862.1:p.Asp1095Val
NM_001289936.1:c.3329A>T , LRG_724t4:c.3329A>T	NP_001276865.1:p.Asp1110Val
NM_001289937.1:c.3160-180A>T	NP_001276866.1:n.3160-180A>T
NM_004448.3:c.3374A>T , LRG_724t2:c.3374A>T	NP_004439.2:p.Asp1125Val
NR_110535.1:n.3698A>T
XM_024450641.1:c.3512A>T	XP_024306409.1:p.Asp1171Val
XM_024450642.1:c.3467A>T	XP_024306410.1:p.Asp1156Val
XM_024450643.1:c.3422A>T	XP_024306411.1:p.Asp1141Val
NM_001005862.3:c.3284A>T	NP_001005862.1:p.Asp1095Val
NM_001289936.2:c.3329A>T	NP_001276865.1:p.Asp1110Val
NM_001289937.2:c.3160-180A>T	NP_001276866.1:n.3160-180A>T
NM_001382782.1:c.3284A>T	NP_001369711.1:p.Asp1095Val
NM_001382783.1:c.3284A>T	NP_001369712.1:p.Asp1095Val
NM_001382784.1:c.3491A>T	NP_001369713.1:p.Asp1164Val
NM_001382785.1:c.3476A>T	NP_001369714.1:p.Asp1159Val
NM_001382786.1:c.3455A>T	NP_001369715.1:p.Asp1152Val
NM_001382787.1:c.3449A>T	NP_001369716.1:p.Asp1150Val
NM_001382788.1:c.3404A>T	NP_001369717.1:p.Asp1135Val
NM_001382789.1:c.3395A>T	NP_001369718.1:p.Asp1132Val
NM_001382790.1:c.3371A>T	NP_001369719.1:p.Asp1124Val
NM_001382791.1:c.3365A>T	NP_001369720.1:p.Asp1122Val
NM_001382792.1:c.3338A>T	NP_001369721.1:p.Asp1113Val
NM_001382793.1:c.3332A>T	NP_001369722.1:p.Asp1111Val
NM_001382794.1:c.3332A>T	NP_001369723.1:p.Asp1111Val
NM_001382795.1:c.3326A>T	NP_001369724.1:p.Asp1109Val
NM_001382796.1:c.3287A>T	NP_001369725.1:p.Asp1096Val
NM_001382797.1:c.3275A>T	NP_001369726.1:p.Asp1092Val
NM_001382798.1:c.3218A>T	NP_001369727.1:p.Asp1073Val
NM_001382799.1:c.3194A>T	NP_001369728.1:p.Asp1065Val
NM_001382800.1:c.3188A>T	NP_001369729.1:p.Asp1063Val
NM_001382801.1:c.3170A>T	NP_001369730.1:p.Asp1057Val
NM_001382802.1:c.3116A>T	NP_001369731.1:p.Asp1039Val
NM_001382803.1:c.3118-180A>T	NP_001369732.1:n.3118-180A>T
NM_001382804.1:c.2546A>T	NP_001369733.1:p.Asp849Val
NM_001382805.1:c.2423A>T	NP_001369734.1:p.Asp808Val
NM_001382806.1:c.2336A>T	NP_001369735.1:p.Asp779Val
NM_004448.4:c.3374A>T MANE Select	NP_004439.2:p.Asp1125Val
NR_110535.2:n.3612A>T