Canonical Allele Identifier: CA399310227

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143235532
• MyVariant Identifiers: chr17:g.37883584T>C (hg19) ; chr17:g.39727331T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727331T>C , CM000679.2:g.39727331T>C	GRCh38
NC_000017.10:g.37883584T>C , CM000679.1:g.37883584T>C	GRCh37
NC_000017.9:g.35137110T>C	NCBI36
NG_007503.1:g.44192T>C , LRG_724:g.44192T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3196T>C MANE Select	ENSP00000269571.4:p.Ser1066Pro
ENST00000269571.9:c.3196T>C	ENSP00000269571.4:p.Ser1066Pro
ENST00000406381.6:c.3106T>C	ENSP00000385185.2:p.Ser1036Pro
ENST00000445658.6:c.2368T>C	ENSP00000404047.2:p.Ser790Pro
ENST00000541774.5:c.3151T>C	ENSP00000446466.1:p.Ser1051Pro
ENST00000578373.5:c.*2986T>C	ENSP00000463427.1:n.*2986T>C
ENST00000584450.5:c.3159+328T>C	ENSP00000463714.1:n.3159+328T>C
ENST00000584601.5:c.3106T>C	ENSP00000462438.1:p.Ser1036Pro
NM_001005862.2:c.3106T>C , LRG_724t1:c.3106T>C	NP_001005862.1:p.Ser1036Pro
NM_001289936.1:c.3151T>C , LRG_724t4:c.3151T>C	NP_001276865.1:p.Ser1051Pro
NM_001289937.1:c.3159+328T>C	NP_001276866.1:n.3159+328T>C
NM_004448.3:c.3196T>C , LRG_724t2:c.3196T>C	NP_004439.2:p.Ser1066Pro
NR_110535.1:n.3520T>C
XM_024450641.1:c.3334T>C	XP_024306409.1:p.Ser1112Pro
XM_024450642.1:c.3289T>C	XP_024306410.1:p.Ser1097Pro
XM_024450643.1:c.3244T>C	XP_024306411.1:p.Ser1082Pro
NM_001005862.3:c.3106T>C	NP_001005862.1:p.Ser1036Pro
NM_001289936.2:c.3151T>C	NP_001276865.1:p.Ser1051Pro
NM_001289937.2:c.3159+328T>C	NP_001276866.1:n.3159+328T>C
NM_001382782.1:c.3106T>C	NP_001369711.1:p.Ser1036Pro
NM_001382783.1:c.3106T>C	NP_001369712.1:p.Ser1036Pro
NM_001382784.1:c.3313T>C	NP_001369713.1:p.Ser1105Pro
NM_001382785.1:c.3298T>C	NP_001369714.1:p.Ser1100Pro
NM_001382786.1:c.3277T>C	NP_001369715.1:p.Ser1093Pro
NM_001382787.1:c.3271T>C	NP_001369716.1:p.Ser1091Pro
NM_001382788.1:c.3226T>C	NP_001369717.1:p.Ser1076Pro
NM_001382789.1:c.3217T>C	NP_001369718.1:p.Ser1073Pro
NM_001382790.1:c.3193T>C	NP_001369719.1:p.Ser1065Pro
NM_001382791.1:c.3187T>C	NP_001369720.1:p.Ser1063Pro
NM_001382792.1:c.3160T>C	NP_001369721.1:p.Ser1054Pro
NM_001382793.1:c.3154T>C	NP_001369722.1:p.Ser1052Pro
NM_001382794.1:c.3154T>C	NP_001369723.1:p.Ser1052Pro
NM_001382795.1:c.3148T>C	NP_001369724.1:p.Ser1050Pro
NM_001382796.1:c.3109T>C	NP_001369725.1:p.Ser1037Pro
NM_001382797.1:c.3097T>C	NP_001369726.1:p.Ser1033Pro
NM_001382798.1:c.3040T>C	NP_001369727.1:p.Ser1014Pro
NM_001382799.1:c.3016T>C	NP_001369728.1:p.Ser1006Pro
NM_001382800.1:c.3010T>C	NP_001369729.1:p.Ser1004Pro
NM_001382801.1:c.2992T>C	NP_001369730.1:p.Ser998Pro
NM_001382802.1:c.2938T>C	NP_001369731.1:p.Ser980Pro
NM_001382803.1:c.3117+328T>C	NP_001369732.1:n.3117+328T>C
NM_001382804.1:c.2368T>C	NP_001369733.1:p.Ser790Pro
NM_001382805.1:c.2245T>C	NP_001369734.1:p.Ser749Pro
NM_001382806.1:c.2158T>C	NP_001369735.1:p.Ser720Pro
NM_004448.4:c.3196T>C MANE Select	NP_004439.2:p.Ser1066Pro
NR_110535.2:n.3434T>C