Canonical Allele Identifier: CA399312572

Gene: ERBB2

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3338G>A MANE Select	ENSP00000269571.4:p.Ser1113Asn
ENST00000269571.9:c.3338G>A	ENSP00000269571.4:p.Ser1113Asn
ENST00000406381.6:c.3248G>A	ENSP00000385185.2:p.Ser1083Asn
ENST00000445658.6:c.2510G>A	ENSP00000404047.2:p.Ser837Asn
ENST00000541774.5:c.3293G>A	ENSP00000446466.1:p.Ser1098Asn
ENST00000578373.5:c.*3128G>A	ENSP00000463427.1:n.*3128G>A
ENST00000584450.5:c.3160-216G>A	ENSP00000463714.1:n.3160-216G>A
ENST00000584601.5:c.3248G>A	ENSP00000462438.1:p.Ser1083Asn
NM_001005862.2:c.3248G>A , LRG_724t1:c.3248G>A	NP_001005862.1:p.Ser1083Asn
NM_001289936.1:c.3293G>A , LRG_724t4:c.3293G>A	NP_001276865.1:p.Ser1098Asn
NM_001289937.1:c.3160-216G>A	NP_001276866.1:n.3160-216G>A
NM_004448.3:c.3338G>A , LRG_724t2:c.3338G>A	NP_004439.2:p.Ser1113Asn
NR_110535.1:n.3662G>A
XM_024450641.1:c.3476G>A	XP_024306409.1:p.Ser1159Asn
XM_024450642.1:c.3431G>A	XP_024306410.1:p.Ser1144Asn
XM_024450643.1:c.3386G>A	XP_024306411.1:p.Ser1129Asn
NM_001005862.3:c.3248G>A	NP_001005862.1:p.Ser1083Asn
NM_001289936.2:c.3293G>A	NP_001276865.1:p.Ser1098Asn
NM_001289937.2:c.3160-216G>A	NP_001276866.1:n.3160-216G>A
NM_001382782.1:c.3248G>A	NP_001369711.1:p.Ser1083Asn
NM_001382783.1:c.3248G>A	NP_001369712.1:p.Ser1083Asn
NM_001382784.1:c.3455G>A	NP_001369713.1:p.Ser1152Asn
NM_001382785.1:c.3440G>A	NP_001369714.1:p.Ser1147Asn
NM_001382786.1:c.3419G>A	NP_001369715.1:p.Ser1140Asn
NM_001382787.1:c.3413G>A	NP_001369716.1:p.Ser1138Asn
NM_001382788.1:c.3368G>A	NP_001369717.1:p.Ser1123Asn
NM_001382789.1:c.3359G>A	NP_001369718.1:p.Ser1120Asn
NM_001382790.1:c.3335G>A	NP_001369719.1:p.Ser1112Asn
NM_001382791.1:c.3329G>A	NP_001369720.1:p.Ser1110Asn
NM_001382792.1:c.3302G>A	NP_001369721.1:p.Ser1101Asn
NM_001382793.1:c.3296G>A	NP_001369722.1:p.Ser1099Asn
NM_001382794.1:c.3296G>A	NP_001369723.1:p.Ser1099Asn
NM_001382795.1:c.3290G>A	NP_001369724.1:p.Ser1097Asn
NM_001382796.1:c.3251G>A	NP_001369725.1:p.Ser1084Asn
NM_001382797.1:c.3239G>A	NP_001369726.1:p.Ser1080Asn
NM_001382798.1:c.3182G>A	NP_001369727.1:p.Ser1061Asn
NM_001382799.1:c.3158G>A	NP_001369728.1:p.Ser1053Asn
NM_001382800.1:c.3152G>A	NP_001369729.1:p.Ser1051Asn
NM_001382801.1:c.3134G>A	NP_001369730.1:p.Ser1045Asn
NM_001382802.1:c.3080G>A	NP_001369731.1:p.Ser1027Asn
NM_001382803.1:c.3118-216G>A	NP_001369732.1:n.3118-216G>A
NM_001382804.1:c.2510G>A	NP_001369733.1:p.Ser837Asn
NM_001382805.1:c.2387G>A	NP_001369734.1:p.Ser796Asn
NM_001382806.1:c.2300G>A	NP_001369735.1:p.Ser767Asn
NM_004448.4:c.3338G>A MANE Select	NP_004439.2:p.Ser1113Asn
NR_110535.2:n.3576G>A