Canonical Allele Identifier: CA399310667

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37883663T>A (hg19) ; chr17:g.39727410T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727410T>A , CM000679.2:g.39727410T>A	GRCh38
NC_000017.10:g.37883663T>A , CM000679.1:g.37883663T>A	GRCh37
NC_000017.9:g.35137189T>A	NCBI36
NG_007503.1:g.44271T>A , LRG_724:g.44271T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3275T>A MANE Select	ENSP00000269571.4:p.Met1092Lys
ENST00000269571.9:c.3275T>A	ENSP00000269571.4:p.Met1092Lys
ENST00000406381.6:c.3185T>A	ENSP00000385185.2:p.Met1062Lys
ENST00000445658.6:c.2447T>A	ENSP00000404047.2:p.Met816Lys
ENST00000541774.5:c.3230T>A	ENSP00000446466.1:p.Met1077Lys
ENST00000578373.5:c.*3065T>A	ENSP00000463427.1:n.*3065T>A
ENST00000584450.5:c.3160-279T>A	ENSP00000463714.1:n.3160-279T>A
ENST00000584601.5:c.3185T>A	ENSP00000462438.1:p.Met1062Lys
NM_001005862.2:c.3185T>A , LRG_724t1:c.3185T>A	NP_001005862.1:p.Met1062Lys
NM_001289936.1:c.3230T>A , LRG_724t4:c.3230T>A	NP_001276865.1:p.Met1077Lys
NM_001289937.1:c.3160-279T>A	NP_001276866.1:n.3160-279T>A
NM_004448.3:c.3275T>A , LRG_724t2:c.3275T>A	NP_004439.2:p.Met1092Lys
NR_110535.1:n.3599T>A
XM_024450641.1:c.3413T>A	XP_024306409.1:p.Met1138Lys
XM_024450642.1:c.3368T>A	XP_024306410.1:p.Met1123Lys
XM_024450643.1:c.3323T>A	XP_024306411.1:p.Met1108Lys
NM_001005862.3:c.3185T>A	NP_001005862.1:p.Met1062Lys
NM_001289936.2:c.3230T>A	NP_001276865.1:p.Met1077Lys
NM_001289937.2:c.3160-279T>A	NP_001276866.1:n.3160-279T>A
NM_001382782.1:c.3185T>A	NP_001369711.1:p.Met1062Lys
NM_001382783.1:c.3185T>A	NP_001369712.1:p.Met1062Lys
NM_001382784.1:c.3392T>A	NP_001369713.1:p.Met1131Lys
NM_001382785.1:c.3377T>A	NP_001369714.1:p.Met1126Lys
NM_001382786.1:c.3356T>A	NP_001369715.1:p.Met1119Lys
NM_001382787.1:c.3350T>A	NP_001369716.1:p.Met1117Lys
NM_001382788.1:c.3305T>A	NP_001369717.1:p.Met1102Lys
NM_001382789.1:c.3296T>A	NP_001369718.1:p.Met1099Lys
NM_001382790.1:c.3272T>A	NP_001369719.1:p.Met1091Lys
NM_001382791.1:c.3266T>A	NP_001369720.1:p.Met1089Lys
NM_001382792.1:c.3239T>A	NP_001369721.1:p.Met1080Lys
NM_001382793.1:c.3233T>A	NP_001369722.1:p.Met1078Lys
NM_001382794.1:c.3233T>A	NP_001369723.1:p.Met1078Lys
NM_001382795.1:c.3227T>A	NP_001369724.1:p.Met1076Lys
NM_001382796.1:c.3188T>A	NP_001369725.1:p.Met1063Lys
NM_001382797.1:c.3176T>A	NP_001369726.1:p.Met1059Lys
NM_001382798.1:c.3119T>A	NP_001369727.1:p.Met1040Lys
NM_001382799.1:c.3095T>A	NP_001369728.1:p.Met1032Lys
NM_001382800.1:c.3089T>A	NP_001369729.1:p.Met1030Lys
NM_001382801.1:c.3071T>A	NP_001369730.1:p.Met1024Lys
NM_001382802.1:c.3017T>A	NP_001369731.1:p.Met1006Lys
NM_001382803.1:c.3118-279T>A	NP_001369732.1:n.3118-279T>A
NM_001382804.1:c.2447T>A	NP_001369733.1:p.Met816Lys
NM_001382805.1:c.2324T>A	NP_001369734.1:p.Met775Lys
NM_001382806.1:c.2237T>A	NP_001369735.1:p.Met746Lys
NM_004448.4:c.3275T>A MANE Select	NP_004439.2:p.Met1092Lys
NR_110535.2:n.3513T>A