Canonical Allele Identifier: CA399310670

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37883664G>T (hg19) ; chr17:g.39727411G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727411G>T , CM000679.2:g.39727411G>T	GRCh38
NC_000017.10:g.37883664G>T , CM000679.1:g.37883664G>T	GRCh37
NC_000017.9:g.35137190G>T	NCBI36
NG_007503.1:g.44272G>T , LRG_724:g.44272G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3276G>T MANE Select	ENSP00000269571.4:p.Met1092Ile
ENST00000269571.9:c.3276G>T	ENSP00000269571.4:p.Met1092Ile
ENST00000406381.6:c.3186G>T	ENSP00000385185.2:p.Met1062Ile
ENST00000445658.6:c.2448G>T	ENSP00000404047.2:p.Met816Ile
ENST00000541774.5:c.3231G>T	ENSP00000446466.1:p.Met1077Ile
ENST00000578373.5:c.*3066G>T	ENSP00000463427.1:n.*3066G>T
ENST00000584450.5:c.3160-278G>T	ENSP00000463714.1:n.3160-278G>T
ENST00000584601.5:c.3186G>T	ENSP00000462438.1:p.Met1062Ile
NM_001005862.2:c.3186G>T , LRG_724t1:c.3186G>T	NP_001005862.1:p.Met1062Ile
NM_001289936.1:c.3231G>T , LRG_724t4:c.3231G>T	NP_001276865.1:p.Met1077Ile
NM_001289937.1:c.3160-278G>T	NP_001276866.1:n.3160-278G>T
NM_004448.3:c.3276G>T , LRG_724t2:c.3276G>T	NP_004439.2:p.Met1092Ile
NR_110535.1:n.3600G>T
XM_024450641.1:c.3414G>T	XP_024306409.1:p.Met1138Ile
XM_024450642.1:c.3369G>T	XP_024306410.1:p.Met1123Ile
XM_024450643.1:c.3324G>T	XP_024306411.1:p.Met1108Ile
NM_001005862.3:c.3186G>T	NP_001005862.1:p.Met1062Ile
NM_001289936.2:c.3231G>T	NP_001276865.1:p.Met1077Ile
NM_001289937.2:c.3160-278G>T	NP_001276866.1:n.3160-278G>T
NM_001382782.1:c.3186G>T	NP_001369711.1:p.Met1062Ile
NM_001382783.1:c.3186G>T	NP_001369712.1:p.Met1062Ile
NM_001382784.1:c.3393G>T	NP_001369713.1:p.Met1131Ile
NM_001382785.1:c.3378G>T	NP_001369714.1:p.Met1126Ile
NM_001382786.1:c.3357G>T	NP_001369715.1:p.Met1119Ile
NM_001382787.1:c.3351G>T	NP_001369716.1:p.Met1117Ile
NM_001382788.1:c.3306G>T	NP_001369717.1:p.Met1102Ile
NM_001382789.1:c.3297G>T	NP_001369718.1:p.Met1099Ile
NM_001382790.1:c.3273G>T	NP_001369719.1:p.Met1091Ile
NM_001382791.1:c.3267G>T	NP_001369720.1:p.Met1089Ile
NM_001382792.1:c.3240G>T	NP_001369721.1:p.Met1080Ile
NM_001382793.1:c.3234G>T	NP_001369722.1:p.Met1078Ile
NM_001382794.1:c.3234G>T	NP_001369723.1:p.Met1078Ile
NM_001382795.1:c.3228G>T	NP_001369724.1:p.Met1076Ile
NM_001382796.1:c.3189G>T	NP_001369725.1:p.Met1063Ile
NM_001382797.1:c.3177G>T	NP_001369726.1:p.Met1059Ile
NM_001382798.1:c.3120G>T	NP_001369727.1:p.Met1040Ile
NM_001382799.1:c.3096G>T	NP_001369728.1:p.Met1032Ile
NM_001382800.1:c.3090G>T	NP_001369729.1:p.Met1030Ile
NM_001382801.1:c.3072G>T	NP_001369730.1:p.Met1024Ile
NM_001382802.1:c.3018G>T	NP_001369731.1:p.Met1006Ile
NM_001382803.1:c.3118-278G>T	NP_001369732.1:n.3118-278G>T
NM_001382804.1:c.2448G>T	NP_001369733.1:p.Met816Ile
NM_001382805.1:c.2325G>T	NP_001369734.1:p.Met775Ile
NM_001382806.1:c.2238G>T	NP_001369735.1:p.Met746Ile
NM_004448.4:c.3276G>T MANE Select	NP_004439.2:p.Met1092Ile
NR_110535.2:n.3514G>T