Canonical Allele Identifier: CA399310346

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37883608C>A (hg19) ; chr17:g.39727355C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727355C>A , CM000679.2:g.39727355C>A	GRCh38
NC_000017.10:g.37883608C>A , CM000679.1:g.37883608C>A	GRCh37
NC_000017.9:g.35137134C>A	NCBI36
NG_007503.1:g.44216C>A , LRG_724:g.44216C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3220C>A MANE Select	ENSP00000269571.4:p.Pro1074Thr
ENST00000269571.9:c.3220C>A	ENSP00000269571.4:p.Pro1074Thr
ENST00000406381.6:c.3130C>A	ENSP00000385185.2:p.Pro1044Thr
ENST00000445658.6:c.2392C>A	ENSP00000404047.2:p.Pro798Thr
ENST00000541774.5:c.3175C>A	ENSP00000446466.1:p.Pro1059Thr
ENST00000578373.5:c.*3010C>A	ENSP00000463427.1:n.*3010C>A
ENST00000584450.5:c.3160-334C>A	ENSP00000463714.1:n.3160-334C>A
ENST00000584601.5:c.3130C>A	ENSP00000462438.1:p.Pro1044Thr
NM_001005862.2:c.3130C>A , LRG_724t1:c.3130C>A	NP_001005862.1:p.Pro1044Thr
NM_001289936.1:c.3175C>A , LRG_724t4:c.3175C>A	NP_001276865.1:p.Pro1059Thr
NM_001289937.1:c.3160-334C>A	NP_001276866.1:n.3160-334C>A
NM_004448.3:c.3220C>A , LRG_724t2:c.3220C>A	NP_004439.2:p.Pro1074Thr
NR_110535.1:n.3544C>A
XM_024450641.1:c.3358C>A	XP_024306409.1:p.Pro1120Thr
XM_024450642.1:c.3313C>A	XP_024306410.1:p.Pro1105Thr
XM_024450643.1:c.3268C>A	XP_024306411.1:p.Pro1090Thr
NM_001005862.3:c.3130C>A	NP_001005862.1:p.Pro1044Thr
NM_001289936.2:c.3175C>A	NP_001276865.1:p.Pro1059Thr
NM_001289937.2:c.3160-334C>A	NP_001276866.1:n.3160-334C>A
NM_001382782.1:c.3130C>A	NP_001369711.1:p.Pro1044Thr
NM_001382783.1:c.3130C>A	NP_001369712.1:p.Pro1044Thr
NM_001382784.1:c.3337C>A	NP_001369713.1:p.Pro1113Thr
NM_001382785.1:c.3322C>A	NP_001369714.1:p.Pro1108Thr
NM_001382786.1:c.3301C>A	NP_001369715.1:p.Pro1101Thr
NM_001382787.1:c.3295C>A	NP_001369716.1:p.Pro1099Thr
NM_001382788.1:c.3250C>A	NP_001369717.1:p.Pro1084Thr
NM_001382789.1:c.3241C>A	NP_001369718.1:p.Pro1081Thr
NM_001382790.1:c.3217C>A	NP_001369719.1:p.Pro1073Thr
NM_001382791.1:c.3211C>A	NP_001369720.1:p.Pro1071Thr
NM_001382792.1:c.3184C>A	NP_001369721.1:p.Pro1062Thr
NM_001382793.1:c.3178C>A	NP_001369722.1:p.Pro1060Thr
NM_001382794.1:c.3178C>A	NP_001369723.1:p.Pro1060Thr
NM_001382795.1:c.3172C>A	NP_001369724.1:p.Pro1058Thr
NM_001382796.1:c.3133C>A	NP_001369725.1:p.Pro1045Thr
NM_001382797.1:c.3121C>A	NP_001369726.1:p.Pro1041Thr
NM_001382798.1:c.3064C>A	NP_001369727.1:p.Pro1022Thr
NM_001382799.1:c.3040C>A	NP_001369728.1:p.Pro1014Thr
NM_001382800.1:c.3034C>A	NP_001369729.1:p.Pro1012Thr
NM_001382801.1:c.3016C>A	NP_001369730.1:p.Pro1006Thr
NM_001382802.1:c.2962C>A	NP_001369731.1:p.Pro988Thr
NM_001382803.1:c.3118-334C>A	NP_001369732.1:n.3118-334C>A
NM_001382804.1:c.2392C>A	NP_001369733.1:p.Pro798Thr
NM_001382805.1:c.2269C>A	NP_001369734.1:p.Pro757Thr
NM_001382806.1:c.2182C>A	NP_001369735.1:p.Pro728Thr
NM_004448.4:c.3220C>A MANE Select	NP_004439.2:p.Pro1074Thr
NR_110535.2:n.3458C>A