Canonical Allele Identifier: CA399312709

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143256280
• MyVariant Identifiers: chr17:g.37883761G>C (hg19) ; chr17:g.39727508G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727508G>C , CM000679.2:g.39727508G>C	GRCh38
NC_000017.10:g.37883761G>C , CM000679.1:g.37883761G>C	GRCh37
NC_000017.9:g.35137287G>C	NCBI36
NG_007503.1:g.44369G>C , LRG_724:g.44369G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3373G>C MANE Select	ENSP00000269571.4:p.Asp1125His
ENST00000269571.9:c.3373G>C	ENSP00000269571.4:p.Asp1125His
ENST00000406381.6:c.3283G>C	ENSP00000385185.2:p.Asp1095His
ENST00000445658.6:c.2545G>C	ENSP00000404047.2:p.Asp849His
ENST00000541774.5:c.3328G>C	ENSP00000446466.1:p.Asp1110His
ENST00000578373.5:c.*3163G>C	ENSP00000463427.1:n.*3163G>C
ENST00000584450.5:c.3160-181G>C	ENSP00000463714.1:n.3160-181G>C
ENST00000584601.5:c.3283G>C	ENSP00000462438.1:p.Asp1095His
NM_001005862.2:c.3283G>C , LRG_724t1:c.3283G>C	NP_001005862.1:p.Asp1095His
NM_001289936.1:c.3328G>C , LRG_724t4:c.3328G>C	NP_001276865.1:p.Asp1110His
NM_001289937.1:c.3160-181G>C	NP_001276866.1:n.3160-181G>C
NM_004448.3:c.3373G>C , LRG_724t2:c.3373G>C	NP_004439.2:p.Asp1125His
NR_110535.1:n.3697G>C
XM_024450641.1:c.3511G>C	XP_024306409.1:p.Asp1171His
XM_024450642.1:c.3466G>C	XP_024306410.1:p.Asp1156His
XM_024450643.1:c.3421G>C	XP_024306411.1:p.Asp1141His
NM_001005862.3:c.3283G>C	NP_001005862.1:p.Asp1095His
NM_001289936.2:c.3328G>C	NP_001276865.1:p.Asp1110His
NM_001289937.2:c.3160-181G>C	NP_001276866.1:n.3160-181G>C
NM_001382782.1:c.3283G>C	NP_001369711.1:p.Asp1095His
NM_001382783.1:c.3283G>C	NP_001369712.1:p.Asp1095His
NM_001382784.1:c.3490G>C	NP_001369713.1:p.Asp1164His
NM_001382785.1:c.3475G>C	NP_001369714.1:p.Asp1159His
NM_001382786.1:c.3454G>C	NP_001369715.1:p.Asp1152His
NM_001382787.1:c.3448G>C	NP_001369716.1:p.Asp1150His
NM_001382788.1:c.3403G>C	NP_001369717.1:p.Asp1135His
NM_001382789.1:c.3394G>C	NP_001369718.1:p.Asp1132His
NM_001382790.1:c.3370G>C	NP_001369719.1:p.Asp1124His
NM_001382791.1:c.3364G>C	NP_001369720.1:p.Asp1122His
NM_001382792.1:c.3337G>C	NP_001369721.1:p.Asp1113His
NM_001382793.1:c.3331G>C	NP_001369722.1:p.Asp1111His
NM_001382794.1:c.3331G>C	NP_001369723.1:p.Asp1111His
NM_001382795.1:c.3325G>C	NP_001369724.1:p.Asp1109His
NM_001382796.1:c.3286G>C	NP_001369725.1:p.Asp1096His
NM_001382797.1:c.3274G>C	NP_001369726.1:p.Asp1092His
NM_001382798.1:c.3217G>C	NP_001369727.1:p.Asp1073His
NM_001382799.1:c.3193G>C	NP_001369728.1:p.Asp1065His
NM_001382800.1:c.3187G>C	NP_001369729.1:p.Asp1063His
NM_001382801.1:c.3169G>C	NP_001369730.1:p.Asp1057His
NM_001382802.1:c.3115G>C	NP_001369731.1:p.Asp1039His
NM_001382803.1:c.3118-181G>C	NP_001369732.1:n.3118-181G>C
NM_001382804.1:c.2545G>C	NP_001369733.1:p.Asp849His
NM_001382805.1:c.2422G>C	NP_001369734.1:p.Asp808His
NM_001382806.1:c.2335G>C	NP_001369735.1:p.Asp779His
NM_004448.4:c.3373G>C MANE Select	NP_004439.2:p.Asp1125His
NR_110535.2:n.3611G>C