Canonical Allele Identifier: CA399312569

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37883726G>T (hg19) ; chr17:g.39727473G>T (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3338G>T MANE Select	ENSP00000269571.4:p.Ser1113Ile
ENST00000269571.9:c.3338G>T	ENSP00000269571.4:p.Ser1113Ile
ENST00000406381.6:c.3248G>T	ENSP00000385185.2:p.Ser1083Ile
ENST00000445658.6:c.2510G>T	ENSP00000404047.2:p.Ser837Ile
ENST00000541774.5:c.3293G>T	ENSP00000446466.1:p.Ser1098Ile
ENST00000578373.5:c.*3128G>T	ENSP00000463427.1:n.*3128G>T
ENST00000584450.5:c.3160-216G>T	ENSP00000463714.1:n.3160-216G>T
ENST00000584601.5:c.3248G>T	ENSP00000462438.1:p.Ser1083Ile
NM_001005862.2:c.3248G>T , LRG_724t1:c.3248G>T	NP_001005862.1:p.Ser1083Ile
NM_001289936.1:c.3293G>T , LRG_724t4:c.3293G>T	NP_001276865.1:p.Ser1098Ile
NM_001289937.1:c.3160-216G>T	NP_001276866.1:n.3160-216G>T
NM_004448.3:c.3338G>T , LRG_724t2:c.3338G>T	NP_004439.2:p.Ser1113Ile
NR_110535.1:n.3662G>T
XM_024450641.1:c.3476G>T	XP_024306409.1:p.Ser1159Ile
XM_024450642.1:c.3431G>T	XP_024306410.1:p.Ser1144Ile
XM_024450643.1:c.3386G>T	XP_024306411.1:p.Ser1129Ile
NM_001005862.3:c.3248G>T	NP_001005862.1:p.Ser1083Ile
NM_001289936.2:c.3293G>T	NP_001276865.1:p.Ser1098Ile
NM_001289937.2:c.3160-216G>T	NP_001276866.1:n.3160-216G>T
NM_001382782.1:c.3248G>T	NP_001369711.1:p.Ser1083Ile
NM_001382783.1:c.3248G>T	NP_001369712.1:p.Ser1083Ile
NM_001382784.1:c.3455G>T	NP_001369713.1:p.Ser1152Ile
NM_001382785.1:c.3440G>T	NP_001369714.1:p.Ser1147Ile
NM_001382786.1:c.3419G>T	NP_001369715.1:p.Ser1140Ile
NM_001382787.1:c.3413G>T	NP_001369716.1:p.Ser1138Ile
NM_001382788.1:c.3368G>T	NP_001369717.1:p.Ser1123Ile
NM_001382789.1:c.3359G>T	NP_001369718.1:p.Ser1120Ile
NM_001382790.1:c.3335G>T	NP_001369719.1:p.Ser1112Ile
NM_001382791.1:c.3329G>T	NP_001369720.1:p.Ser1110Ile
NM_001382792.1:c.3302G>T	NP_001369721.1:p.Ser1101Ile
NM_001382793.1:c.3296G>T	NP_001369722.1:p.Ser1099Ile
NM_001382794.1:c.3296G>T	NP_001369723.1:p.Ser1099Ile
NM_001382795.1:c.3290G>T	NP_001369724.1:p.Ser1097Ile
NM_001382796.1:c.3251G>T	NP_001369725.1:p.Ser1084Ile
NM_001382797.1:c.3239G>T	NP_001369726.1:p.Ser1080Ile
NM_001382798.1:c.3182G>T	NP_001369727.1:p.Ser1061Ile
NM_001382799.1:c.3158G>T	NP_001369728.1:p.Ser1053Ile
NM_001382800.1:c.3152G>T	NP_001369729.1:p.Ser1051Ile
NM_001382801.1:c.3134G>T	NP_001369730.1:p.Ser1045Ile
NM_001382802.1:c.3080G>T	NP_001369731.1:p.Ser1027Ile
NM_001382803.1:c.3118-216G>T	NP_001369732.1:n.3118-216G>T
NM_001382804.1:c.2510G>T	NP_001369733.1:p.Ser837Ile
NM_001382805.1:c.2387G>T	NP_001369734.1:p.Ser796Ile
NM_001382806.1:c.2300G>T	NP_001369735.1:p.Ser767Ile
NM_004448.4:c.3338G>T MANE Select	NP_004439.2:p.Ser1113Ile
NR_110535.2:n.3576G>T