Canonical Allele Identifier: CA399312570

Gene: ERBB2

Linked Data

• dbSNP Id: rs2059840010
• MyVariant Identifiers: chr17:g.37883726G>C (hg19) ; chr17:g.39727473G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727473G>C , CM000679.2:g.39727473G>C	GRCh38
NC_000017.10:g.37883726G>C , CM000679.1:g.37883726G>C	GRCh37
NC_000017.9:g.35137252G>C	NCBI36
NG_007503.1:g.44334G>C , LRG_724:g.44334G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3338G>C MANE Select	ENSP00000269571.4:p.Ser1113Thr
ENST00000269571.9:c.3338G>C	ENSP00000269571.4:p.Ser1113Thr
ENST00000406381.6:c.3248G>C	ENSP00000385185.2:p.Ser1083Thr
ENST00000445658.6:c.2510G>C	ENSP00000404047.2:p.Ser837Thr
ENST00000541774.5:c.3293G>C	ENSP00000446466.1:p.Ser1098Thr
ENST00000578373.5:c.*3128G>C	ENSP00000463427.1:n.*3128G>C
ENST00000584450.5:c.3160-216G>C	ENSP00000463714.1:n.3160-216G>C
ENST00000584601.5:c.3248G>C	ENSP00000462438.1:p.Ser1083Thr
NM_001005862.2:c.3248G>C , LRG_724t1:c.3248G>C	NP_001005862.1:p.Ser1083Thr
NM_001289936.1:c.3293G>C , LRG_724t4:c.3293G>C	NP_001276865.1:p.Ser1098Thr
NM_001289937.1:c.3160-216G>C	NP_001276866.1:n.3160-216G>C
NM_004448.3:c.3338G>C , LRG_724t2:c.3338G>C	NP_004439.2:p.Ser1113Thr
NR_110535.1:n.3662G>C
XM_024450641.1:c.3476G>C	XP_024306409.1:p.Ser1159Thr
XM_024450642.1:c.3431G>C	XP_024306410.1:p.Ser1144Thr
XM_024450643.1:c.3386G>C	XP_024306411.1:p.Ser1129Thr
NM_001005862.3:c.3248G>C	NP_001005862.1:p.Ser1083Thr
NM_001289936.2:c.3293G>C	NP_001276865.1:p.Ser1098Thr
NM_001289937.2:c.3160-216G>C	NP_001276866.1:n.3160-216G>C
NM_001382782.1:c.3248G>C	NP_001369711.1:p.Ser1083Thr
NM_001382783.1:c.3248G>C	NP_001369712.1:p.Ser1083Thr
NM_001382784.1:c.3455G>C	NP_001369713.1:p.Ser1152Thr
NM_001382785.1:c.3440G>C	NP_001369714.1:p.Ser1147Thr
NM_001382786.1:c.3419G>C	NP_001369715.1:p.Ser1140Thr
NM_001382787.1:c.3413G>C	NP_001369716.1:p.Ser1138Thr
NM_001382788.1:c.3368G>C	NP_001369717.1:p.Ser1123Thr
NM_001382789.1:c.3359G>C	NP_001369718.1:p.Ser1120Thr
NM_001382790.1:c.3335G>C	NP_001369719.1:p.Ser1112Thr
NM_001382791.1:c.3329G>C	NP_001369720.1:p.Ser1110Thr
NM_001382792.1:c.3302G>C	NP_001369721.1:p.Ser1101Thr
NM_001382793.1:c.3296G>C	NP_001369722.1:p.Ser1099Thr
NM_001382794.1:c.3296G>C	NP_001369723.1:p.Ser1099Thr
NM_001382795.1:c.3290G>C	NP_001369724.1:p.Ser1097Thr
NM_001382796.1:c.3251G>C	NP_001369725.1:p.Ser1084Thr
NM_001382797.1:c.3239G>C	NP_001369726.1:p.Ser1080Thr
NM_001382798.1:c.3182G>C	NP_001369727.1:p.Ser1061Thr
NM_001382799.1:c.3158G>C	NP_001369728.1:p.Ser1053Thr
NM_001382800.1:c.3152G>C	NP_001369729.1:p.Ser1051Thr
NM_001382801.1:c.3134G>C	NP_001369730.1:p.Ser1045Thr
NM_001382802.1:c.3080G>C	NP_001369731.1:p.Ser1027Thr
NM_001382803.1:c.3118-216G>C	NP_001369732.1:n.3118-216G>C
NM_001382804.1:c.2510G>C	NP_001369733.1:p.Ser837Thr
NM_001382805.1:c.2387G>C	NP_001369734.1:p.Ser796Thr
NM_001382806.1:c.2300G>C	NP_001369735.1:p.Ser767Thr
NM_004448.4:c.3338G>C MANE Select	NP_004439.2:p.Ser1113Thr
NR_110535.2:n.3576G>C