Canonical Allele Identifier: CA399312736

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37883767T>G (hg19) ; chr17:g.39727514T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727514T>G , CM000679.2:g.39727514T>G	GRCh38
NC_000017.10:g.37883767T>G , CM000679.1:g.37883767T>G	GRCh37
NC_000017.9:g.35137293T>G	NCBI36
NG_007503.1:g.44375T>G , LRG_724:g.44375T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3379T>G MANE Select	ENSP00000269571.4:p.Tyr1127Asp
ENST00000269571.9:c.3379T>G	ENSP00000269571.4:p.Tyr1127Asp
ENST00000406381.6:c.3289T>G	ENSP00000385185.2:p.Tyr1097Asp
ENST00000445658.6:c.2551T>G	ENSP00000404047.2:p.Tyr851Asp
ENST00000541774.5:c.3334T>G	ENSP00000446466.1:p.Tyr1112Asp
ENST00000578373.5:c.*3169T>G	ENSP00000463427.1:n.*3169T>G
ENST00000584450.5:c.3160-175T>G	ENSP00000463714.1:n.3160-175T>G
ENST00000584601.5:c.3289T>G	ENSP00000462438.1:p.Tyr1097Asp
NM_001005862.2:c.3289T>G , LRG_724t1:c.3289T>G	NP_001005862.1:p.Tyr1097Asp
NM_001289936.1:c.3334T>G , LRG_724t4:c.3334T>G	NP_001276865.1:p.Tyr1112Asp
NM_001289937.1:c.3160-175T>G	NP_001276866.1:n.3160-175T>G
NM_004448.3:c.3379T>G , LRG_724t2:c.3379T>G	NP_004439.2:p.Tyr1127Asp
NR_110535.1:n.3703T>G
XM_024450641.1:c.3517T>G	XP_024306409.1:p.Tyr1173Asp
XM_024450642.1:c.3472T>G	XP_024306410.1:p.Tyr1158Asp
XM_024450643.1:c.3427T>G	XP_024306411.1:p.Tyr1143Asp
NM_001005862.3:c.3289T>G	NP_001005862.1:p.Tyr1097Asp
NM_001289936.2:c.3334T>G	NP_001276865.1:p.Tyr1112Asp
NM_001289937.2:c.3160-175T>G	NP_001276866.1:n.3160-175T>G
NM_001382782.1:c.3289T>G	NP_001369711.1:p.Tyr1097Asp
NM_001382783.1:c.3289T>G	NP_001369712.1:p.Tyr1097Asp
NM_001382784.1:c.3496T>G	NP_001369713.1:p.Tyr1166Asp
NM_001382785.1:c.3481T>G	NP_001369714.1:p.Tyr1161Asp
NM_001382786.1:c.3460T>G	NP_001369715.1:p.Tyr1154Asp
NM_001382787.1:c.3454T>G	NP_001369716.1:p.Tyr1152Asp
NM_001382788.1:c.3409T>G	NP_001369717.1:p.Tyr1137Asp
NM_001382789.1:c.3400T>G	NP_001369718.1:p.Tyr1134Asp
NM_001382790.1:c.3376T>G	NP_001369719.1:p.Tyr1126Asp
NM_001382791.1:c.3370T>G	NP_001369720.1:p.Tyr1124Asp
NM_001382792.1:c.3343T>G	NP_001369721.1:p.Tyr1115Asp
NM_001382793.1:c.3337T>G	NP_001369722.1:p.Tyr1113Asp
NM_001382794.1:c.3337T>G	NP_001369723.1:p.Tyr1113Asp
NM_001382795.1:c.3331T>G	NP_001369724.1:p.Tyr1111Asp
NM_001382796.1:c.3292T>G	NP_001369725.1:p.Tyr1098Asp
NM_001382797.1:c.3280T>G	NP_001369726.1:p.Tyr1094Asp
NM_001382798.1:c.3223T>G	NP_001369727.1:p.Tyr1075Asp
NM_001382799.1:c.3199T>G	NP_001369728.1:p.Tyr1067Asp
NM_001382800.1:c.3193T>G	NP_001369729.1:p.Tyr1065Asp
NM_001382801.1:c.3175T>G	NP_001369730.1:p.Tyr1059Asp
NM_001382802.1:c.3121T>G	NP_001369731.1:p.Tyr1041Asp
NM_001382803.1:c.3118-175T>G	NP_001369732.1:n.3118-175T>G
NM_001382804.1:c.2551T>G	NP_001369733.1:p.Tyr851Asp
NM_001382805.1:c.2428T>G	NP_001369734.1:p.Tyr810Asp
NM_001382806.1:c.2341T>G	NP_001369735.1:p.Tyr781Asp
NM_004448.4:c.3379T>G MANE Select	NP_004439.2:p.Tyr1127Asp
NR_110535.2:n.3617T>G