Canonical Allele Identifier: CA399312741

Gene: ERBB2

Linked Data

• dbSNP Id: rs545806496
• MyVariant Identifiers: chr17:g.37883769C>G (hg19) ; chr17:g.39727516C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727516C>G , CM000679.2:g.39727516C>G	GRCh38
NC_000017.10:g.37883769C>G , CM000679.1:g.37883769C>G	GRCh37
NC_000017.9:g.35137295C>G	NCBI36
NG_007503.1:g.44377C>G , LRG_724:g.44377C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3381C>G MANE Select	ENSP00000269571.4:p.Tyr1127Ter
ENST00000269571.9:c.3381C>G	ENSP00000269571.4:p.Tyr1127Ter
ENST00000406381.6:c.3291C>G	ENSP00000385185.2:p.Tyr1097Ter
ENST00000445658.6:c.2553C>G	ENSP00000404047.2:p.Tyr851Ter
ENST00000541774.5:c.3336C>G	ENSP00000446466.1:p.Tyr1112Ter
ENST00000578373.5:c.*3171C>G	ENSP00000463427.1:n.*3171C>G
ENST00000584450.5:c.3160-173C>G	ENSP00000463714.1:n.3160-173C>G
ENST00000584601.5:c.3291C>G	ENSP00000462438.1:p.Tyr1097Ter
NM_001005862.2:c.3291C>G , LRG_724t1:c.3291C>G	NP_001005862.1:p.Tyr1097Ter
NM_001289936.1:c.3336C>G , LRG_724t4:c.3336C>G	NP_001276865.1:p.Tyr1112Ter
NM_001289937.1:c.3160-173C>G	NP_001276866.1:n.3160-173C>G
NM_004448.3:c.3381C>G , LRG_724t2:c.3381C>G	NP_004439.2:p.Tyr1127Ter
NR_110535.1:n.3705C>G
XM_024450641.1:c.3519C>G	XP_024306409.1:p.Tyr1173Ter
XM_024450642.1:c.3474C>G	XP_024306410.1:p.Tyr1158Ter
XM_024450643.1:c.3429C>G	XP_024306411.1:p.Tyr1143Ter
NM_001005862.3:c.3291C>G	NP_001005862.1:p.Tyr1097Ter
NM_001289936.2:c.3336C>G	NP_001276865.1:p.Tyr1112Ter
NM_001289937.2:c.3160-173C>G	NP_001276866.1:n.3160-173C>G
NM_001382782.1:c.3291C>G	NP_001369711.1:p.Tyr1097Ter
NM_001382783.1:c.3291C>G	NP_001369712.1:p.Tyr1097Ter
NM_001382784.1:c.3498C>G	NP_001369713.1:p.Tyr1166Ter
NM_001382785.1:c.3483C>G	NP_001369714.1:p.Tyr1161Ter
NM_001382786.1:c.3462C>G	NP_001369715.1:p.Tyr1154Ter
NM_001382787.1:c.3456C>G	NP_001369716.1:p.Tyr1152Ter
NM_001382788.1:c.3411C>G	NP_001369717.1:p.Tyr1137Ter
NM_001382789.1:c.3402C>G	NP_001369718.1:p.Tyr1134Ter
NM_001382790.1:c.3378C>G	NP_001369719.1:p.Tyr1126Ter
NM_001382791.1:c.3372C>G	NP_001369720.1:p.Tyr1124Ter
NM_001382792.1:c.3345C>G	NP_001369721.1:p.Tyr1115Ter
NM_001382793.1:c.3339C>G	NP_001369722.1:p.Tyr1113Ter
NM_001382794.1:c.3339C>G	NP_001369723.1:p.Tyr1113Ter
NM_001382795.1:c.3333C>G	NP_001369724.1:p.Tyr1111Ter
NM_001382796.1:c.3294C>G	NP_001369725.1:p.Tyr1098Ter
NM_001382797.1:c.3282C>G	NP_001369726.1:p.Tyr1094Ter
NM_001382798.1:c.3225C>G	NP_001369727.1:p.Tyr1075Ter
NM_001382799.1:c.3201C>G	NP_001369728.1:p.Tyr1067Ter
NM_001382800.1:c.3195C>G	NP_001369729.1:p.Tyr1065Ter
NM_001382801.1:c.3177C>G	NP_001369730.1:p.Tyr1059Ter
NM_001382802.1:c.3123C>G	NP_001369731.1:p.Tyr1041Ter
NM_001382803.1:c.3118-173C>G	NP_001369732.1:n.3118-173C>G
NM_001382804.1:c.2553C>G	NP_001369733.1:p.Tyr851Ter
NM_001382805.1:c.2430C>G	NP_001369734.1:p.Tyr810Ter
NM_001382806.1:c.2343C>G	NP_001369735.1:p.Tyr781Ter
NM_004448.4:c.3381C>G MANE Select	NP_004439.2:p.Tyr1127Ter
NR_110535.2:n.3619C>G