Canonical Allele Identifier: CA399310586

Gene: ERBB2

Linked Data

• dbSNP Id: rs2059835022
• MyVariant Identifiers: chr17:g.37883647G>C (hg19) ; chr17:g.39727394G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727394G>C , CM000679.2:g.39727394G>C	GRCh38
NC_000017.10:g.37883647G>C , CM000679.1:g.37883647G>C	GRCh37
NC_000017.9:g.35137173G>C	NCBI36
NG_007503.1:g.44255G>C , LRG_724:g.44255G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3259G>C MANE Select	ENSP00000269571.4:p.Asp1087His
ENST00000269571.9:c.3259G>C	ENSP00000269571.4:p.Asp1087His
ENST00000406381.6:c.3169G>C	ENSP00000385185.2:p.Asp1057His
ENST00000445658.6:c.2431G>C	ENSP00000404047.2:p.Asp811His
ENST00000541774.5:c.3214G>C	ENSP00000446466.1:p.Asp1072His
ENST00000578373.5:c.*3049G>C	ENSP00000463427.1:n.*3049G>C
ENST00000584450.5:c.3160-295G>C	ENSP00000463714.1:n.3160-295G>C
ENST00000584601.5:c.3169G>C	ENSP00000462438.1:p.Asp1057His
NM_001005862.2:c.3169G>C , LRG_724t1:c.3169G>C	NP_001005862.1:p.Asp1057His
NM_001289936.1:c.3214G>C , LRG_724t4:c.3214G>C	NP_001276865.1:p.Asp1072His
NM_001289937.1:c.3160-295G>C	NP_001276866.1:n.3160-295G>C
NM_004448.3:c.3259G>C , LRG_724t2:c.3259G>C	NP_004439.2:p.Asp1087His
NR_110535.1:n.3583G>C
XM_024450641.1:c.3397G>C	XP_024306409.1:p.Asp1133His
XM_024450642.1:c.3352G>C	XP_024306410.1:p.Asp1118His
XM_024450643.1:c.3307G>C	XP_024306411.1:p.Asp1103His
NM_001005862.3:c.3169G>C	NP_001005862.1:p.Asp1057His
NM_001289936.2:c.3214G>C	NP_001276865.1:p.Asp1072His
NM_001289937.2:c.3160-295G>C	NP_001276866.1:n.3160-295G>C
NM_001382782.1:c.3169G>C	NP_001369711.1:p.Asp1057His
NM_001382783.1:c.3169G>C	NP_001369712.1:p.Asp1057His
NM_001382784.1:c.3376G>C	NP_001369713.1:p.Asp1126His
NM_001382785.1:c.3361G>C	NP_001369714.1:p.Asp1121His
NM_001382786.1:c.3340G>C	NP_001369715.1:p.Asp1114His
NM_001382787.1:c.3334G>C	NP_001369716.1:p.Asp1112His
NM_001382788.1:c.3289G>C	NP_001369717.1:p.Asp1097His
NM_001382789.1:c.3280G>C	NP_001369718.1:p.Asp1094His
NM_001382790.1:c.3256G>C	NP_001369719.1:p.Asp1086His
NM_001382791.1:c.3250G>C	NP_001369720.1:p.Asp1084His
NM_001382792.1:c.3223G>C	NP_001369721.1:p.Asp1075His
NM_001382793.1:c.3217G>C	NP_001369722.1:p.Asp1073His
NM_001382794.1:c.3217G>C	NP_001369723.1:p.Asp1073His
NM_001382795.1:c.3211G>C	NP_001369724.1:p.Asp1071His
NM_001382796.1:c.3172G>C	NP_001369725.1:p.Asp1058His
NM_001382797.1:c.3160G>C	NP_001369726.1:p.Asp1054His
NM_001382798.1:c.3103G>C	NP_001369727.1:p.Asp1035His
NM_001382799.1:c.3079G>C	NP_001369728.1:p.Asp1027His
NM_001382800.1:c.3073G>C	NP_001369729.1:p.Asp1025His
NM_001382801.1:c.3055G>C	NP_001369730.1:p.Asp1019His
NM_001382802.1:c.3001G>C	NP_001369731.1:p.Asp1001His
NM_001382803.1:c.3118-295G>C	NP_001369732.1:n.3118-295G>C
NM_001382804.1:c.2431G>C	NP_001369733.1:p.Asp811His
NM_001382805.1:c.2308G>C	NP_001369734.1:p.Asp770His
NM_001382806.1:c.2221G>C	NP_001369735.1:p.Asp741His
NM_004448.4:c.3259G>C MANE Select	NP_004439.2:p.Asp1087His
NR_110535.2:n.3497G>C