Canonical Allele Identifier: CA399310618

Gene: ERBB2

Linked Data

• dbSNP Id: rs749154778
• MyVariant Identifiers: chr17:g.37883651G>C (hg19) ; chr17:g.39727398G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727398G>C , CM000679.2:g.39727398G>C	GRCh38
NC_000017.10:g.37883651G>C , CM000679.1:g.37883651G>C	GRCh37
NC_000017.9:g.35137177G>C	NCBI36
NG_007503.1:g.44259G>C , LRG_724:g.44259G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3263G>C MANE Select	ENSP00000269571.4:p.Gly1088Ala
ENST00000269571.9:c.3263G>C	ENSP00000269571.4:p.Gly1088Ala
ENST00000406381.6:c.3173G>C	ENSP00000385185.2:p.Gly1058Ala
ENST00000445658.6:c.2435G>C	ENSP00000404047.2:p.Gly812Ala
ENST00000541774.5:c.3218G>C	ENSP00000446466.1:p.Gly1073Ala
ENST00000578373.5:c.*3053G>C	ENSP00000463427.1:n.*3053G>C
ENST00000584450.5:c.3160-291G>C	ENSP00000463714.1:n.3160-291G>C
ENST00000584601.5:c.3173G>C	ENSP00000462438.1:p.Gly1058Ala
NM_001005862.2:c.3173G>C , LRG_724t1:c.3173G>C	NP_001005862.1:p.Gly1058Ala
NM_001289936.1:c.3218G>C , LRG_724t4:c.3218G>C	NP_001276865.1:p.Gly1073Ala
NM_001289937.1:c.3160-291G>C	NP_001276866.1:n.3160-291G>C
NM_004448.3:c.3263G>C , LRG_724t2:c.3263G>C	NP_004439.2:p.Gly1088Ala
NR_110535.1:n.3587G>C
XM_024450641.1:c.3401G>C	XP_024306409.1:p.Gly1134Ala
XM_024450642.1:c.3356G>C	XP_024306410.1:p.Gly1119Ala
XM_024450643.1:c.3311G>C	XP_024306411.1:p.Gly1104Ala
NM_001005862.3:c.3173G>C	NP_001005862.1:p.Gly1058Ala
NM_001289936.2:c.3218G>C	NP_001276865.1:p.Gly1073Ala
NM_001289937.2:c.3160-291G>C	NP_001276866.1:n.3160-291G>C
NM_001382782.1:c.3173G>C	NP_001369711.1:p.Gly1058Ala
NM_001382783.1:c.3173G>C	NP_001369712.1:p.Gly1058Ala
NM_001382784.1:c.3380G>C	NP_001369713.1:p.Gly1127Ala
NM_001382785.1:c.3365G>C	NP_001369714.1:p.Gly1122Ala
NM_001382786.1:c.3344G>C	NP_001369715.1:p.Gly1115Ala
NM_001382787.1:c.3338G>C	NP_001369716.1:p.Gly1113Ala
NM_001382788.1:c.3293G>C	NP_001369717.1:p.Gly1098Ala
NM_001382789.1:c.3284G>C	NP_001369718.1:p.Gly1095Ala
NM_001382790.1:c.3260G>C	NP_001369719.1:p.Gly1087Ala
NM_001382791.1:c.3254G>C	NP_001369720.1:p.Gly1085Ala
NM_001382792.1:c.3227G>C	NP_001369721.1:p.Gly1076Ala
NM_001382793.1:c.3221G>C	NP_001369722.1:p.Gly1074Ala
NM_001382794.1:c.3221G>C	NP_001369723.1:p.Gly1074Ala
NM_001382795.1:c.3215G>C	NP_001369724.1:p.Gly1072Ala
NM_001382796.1:c.3176G>C	NP_001369725.1:p.Gly1059Ala
NM_001382797.1:c.3164G>C	NP_001369726.1:p.Gly1055Ala
NM_001382798.1:c.3107G>C	NP_001369727.1:p.Gly1036Ala
NM_001382799.1:c.3083G>C	NP_001369728.1:p.Gly1028Ala
NM_001382800.1:c.3077G>C	NP_001369729.1:p.Gly1026Ala
NM_001382801.1:c.3059G>C	NP_001369730.1:p.Gly1020Ala
NM_001382802.1:c.3005G>C	NP_001369731.1:p.Gly1002Ala
NM_001382803.1:c.3118-291G>C	NP_001369732.1:n.3118-291G>C
NM_001382804.1:c.2435G>C	NP_001369733.1:p.Gly812Ala
NM_001382805.1:c.2312G>C	NP_001369734.1:p.Gly771Ala
NM_001382806.1:c.2225G>C	NP_001369735.1:p.Gly742Ala
NM_004448.4:c.3263G>C MANE Select	NP_004439.2:p.Gly1088Ala
NR_110535.2:n.3501G>C