Canonical Allele Identifier: CA399310971

Gene: ERBB2

Linked Data

• dbSNP Id: rs111611886
• MyVariant Identifiers: chr17:g.37883701G>C (hg19) ; chr17:g.39727448G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727448G>C , CM000679.2:g.39727448G>C	GRCh38
NC_000017.10:g.37883701G>C , CM000679.1:g.37883701G>C	GRCh37
NC_000017.9:g.35137227G>C	NCBI36
NG_007503.1:g.44309G>C , LRG_724:g.44309G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3313G>C MANE Select	ENSP00000269571.4:p.Asp1105His
ENST00000269571.9:c.3313G>C	ENSP00000269571.4:p.Asp1105His
ENST00000406381.6:c.3223G>C	ENSP00000385185.2:p.Asp1075His
ENST00000445658.6:c.2485G>C	ENSP00000404047.2:p.Asp829His
ENST00000541774.5:c.3268G>C	ENSP00000446466.1:p.Asp1090His
ENST00000578373.5:c.*3103G>C	ENSP00000463427.1:n.*3103G>C
ENST00000584450.5:c.3160-241G>C	ENSP00000463714.1:n.3160-241G>C
ENST00000584601.5:c.3223G>C	ENSP00000462438.1:p.Asp1075His
NM_001005862.2:c.3223G>C , LRG_724t1:c.3223G>C	NP_001005862.1:p.Asp1075His
NM_001289936.1:c.3268G>C , LRG_724t4:c.3268G>C	NP_001276865.1:p.Asp1090His
NM_001289937.1:c.3160-241G>C	NP_001276866.1:n.3160-241G>C
NM_004448.3:c.3313G>C , LRG_724t2:c.3313G>C	NP_004439.2:p.Asp1105His
NR_110535.1:n.3637G>C
XM_024450641.1:c.3451G>C	XP_024306409.1:p.Asp1151His
XM_024450642.1:c.3406G>C	XP_024306410.1:p.Asp1136His
XM_024450643.1:c.3361G>C	XP_024306411.1:p.Asp1121His
NM_001005862.3:c.3223G>C	NP_001005862.1:p.Asp1075His
NM_001289936.2:c.3268G>C	NP_001276865.1:p.Asp1090His
NM_001289937.2:c.3160-241G>C	NP_001276866.1:n.3160-241G>C
NM_001382782.1:c.3223G>C	NP_001369711.1:p.Asp1075His
NM_001382783.1:c.3223G>C	NP_001369712.1:p.Asp1075His
NM_001382784.1:c.3430G>C	NP_001369713.1:p.Asp1144His
NM_001382785.1:c.3415G>C	NP_001369714.1:p.Asp1139His
NM_001382786.1:c.3394G>C	NP_001369715.1:p.Asp1132His
NM_001382787.1:c.3388G>C	NP_001369716.1:p.Asp1130His
NM_001382788.1:c.3343G>C	NP_001369717.1:p.Asp1115His
NM_001382789.1:c.3334G>C	NP_001369718.1:p.Asp1112His
NM_001382790.1:c.3310G>C	NP_001369719.1:p.Asp1104His
NM_001382791.1:c.3304G>C	NP_001369720.1:p.Asp1102His
NM_001382792.1:c.3277G>C	NP_001369721.1:p.Asp1093His
NM_001382793.1:c.3271G>C	NP_001369722.1:p.Asp1091His
NM_001382794.1:c.3271G>C	NP_001369723.1:p.Asp1091His
NM_001382795.1:c.3265G>C	NP_001369724.1:p.Asp1089His
NM_001382796.1:c.3226G>C	NP_001369725.1:p.Asp1076His
NM_001382797.1:c.3214G>C	NP_001369726.1:p.Asp1072His
NM_001382798.1:c.3157G>C	NP_001369727.1:p.Asp1053His
NM_001382799.1:c.3133G>C	NP_001369728.1:p.Asp1045His
NM_001382800.1:c.3127G>C	NP_001369729.1:p.Asp1043His
NM_001382801.1:c.3109G>C	NP_001369730.1:p.Asp1037His
NM_001382802.1:c.3055G>C	NP_001369731.1:p.Asp1019His
NM_001382803.1:c.3118-241G>C	NP_001369732.1:n.3118-241G>C
NM_001382804.1:c.2485G>C	NP_001369733.1:p.Asp829His
NM_001382805.1:c.2362G>C	NP_001369734.1:p.Asp788His
NM_001382806.1:c.2275G>C	NP_001369735.1:p.Asp759His
NM_004448.4:c.3313G>C MANE Select	NP_004439.2:p.Asp1105His
NR_110535.2:n.3551G>C