Canonical Allele Identifier: CA399312553

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143252084
• MyVariant Identifiers: chr17:g.37883722T>G (hg19) ; chr17:g.39727469T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727469T>G , CM000679.2:g.39727469T>G	GRCh38
NC_000017.10:g.37883722T>G , CM000679.1:g.37883722T>G	GRCh37
NC_000017.9:g.35137248T>G	NCBI36
NG_007503.1:g.44330T>G , LRG_724:g.44330T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3334T>G MANE Select	ENSP00000269571.4:p.Tyr1112Asp
ENST00000269571.9:c.3334T>G	ENSP00000269571.4:p.Tyr1112Asp
ENST00000406381.6:c.3244T>G	ENSP00000385185.2:p.Tyr1082Asp
ENST00000445658.6:c.2506T>G	ENSP00000404047.2:p.Tyr836Asp
ENST00000541774.5:c.3289T>G	ENSP00000446466.1:p.Tyr1097Asp
ENST00000578373.5:c.*3124T>G	ENSP00000463427.1:n.*3124T>G
ENST00000584450.5:c.3160-220T>G	ENSP00000463714.1:n.3160-220T>G
ENST00000584601.5:c.3244T>G	ENSP00000462438.1:p.Tyr1082Asp
NM_001005862.2:c.3244T>G , LRG_724t1:c.3244T>G	NP_001005862.1:p.Tyr1082Asp
NM_001289936.1:c.3289T>G , LRG_724t4:c.3289T>G	NP_001276865.1:p.Tyr1097Asp
NM_001289937.1:c.3160-220T>G	NP_001276866.1:n.3160-220T>G
NM_004448.3:c.3334T>G , LRG_724t2:c.3334T>G	NP_004439.2:p.Tyr1112Asp
NR_110535.1:n.3658T>G
XM_024450641.1:c.3472T>G	XP_024306409.1:p.Tyr1158Asp
XM_024450642.1:c.3427T>G	XP_024306410.1:p.Tyr1143Asp
XM_024450643.1:c.3382T>G	XP_024306411.1:p.Tyr1128Asp
NM_001005862.3:c.3244T>G	NP_001005862.1:p.Tyr1082Asp
NM_001289936.2:c.3289T>G	NP_001276865.1:p.Tyr1097Asp
NM_001289937.2:c.3160-220T>G	NP_001276866.1:n.3160-220T>G
NM_001382782.1:c.3244T>G	NP_001369711.1:p.Tyr1082Asp
NM_001382783.1:c.3244T>G	NP_001369712.1:p.Tyr1082Asp
NM_001382784.1:c.3451T>G	NP_001369713.1:p.Tyr1151Asp
NM_001382785.1:c.3436T>G	NP_001369714.1:p.Tyr1146Asp
NM_001382786.1:c.3415T>G	NP_001369715.1:p.Tyr1139Asp
NM_001382787.1:c.3409T>G	NP_001369716.1:p.Tyr1137Asp
NM_001382788.1:c.3364T>G	NP_001369717.1:p.Tyr1122Asp
NM_001382789.1:c.3355T>G	NP_001369718.1:p.Tyr1119Asp
NM_001382790.1:c.3331T>G	NP_001369719.1:p.Tyr1111Asp
NM_001382791.1:c.3325T>G	NP_001369720.1:p.Tyr1109Asp
NM_001382792.1:c.3298T>G	NP_001369721.1:p.Tyr1100Asp
NM_001382793.1:c.3292T>G	NP_001369722.1:p.Tyr1098Asp
NM_001382794.1:c.3292T>G	NP_001369723.1:p.Tyr1098Asp
NM_001382795.1:c.3286T>G	NP_001369724.1:p.Tyr1096Asp
NM_001382796.1:c.3247T>G	NP_001369725.1:p.Tyr1083Asp
NM_001382797.1:c.3235T>G	NP_001369726.1:p.Tyr1079Asp
NM_001382798.1:c.3178T>G	NP_001369727.1:p.Tyr1060Asp
NM_001382799.1:c.3154T>G	NP_001369728.1:p.Tyr1052Asp
NM_001382800.1:c.3148T>G	NP_001369729.1:p.Tyr1050Asp
NM_001382801.1:c.3130T>G	NP_001369730.1:p.Tyr1044Asp
NM_001382802.1:c.3076T>G	NP_001369731.1:p.Tyr1026Asp
NM_001382803.1:c.3118-220T>G	NP_001369732.1:n.3118-220T>G
NM_001382804.1:c.2506T>G	NP_001369733.1:p.Tyr836Asp
NM_001382805.1:c.2383T>G	NP_001369734.1:p.Tyr795Asp
NM_001382806.1:c.2296T>G	NP_001369735.1:p.Tyr766Asp
NM_004448.4:c.3334T>G MANE Select	NP_004439.2:p.Tyr1112Asp
NR_110535.2:n.3572T>G