Canonical Allele Identifier: CA399310662

Gene: ERBB2

Linked Data

• dbSNP Id: rs1567916468
• MyVariant Identifiers: chr17:g.37883660G>C (hg19) ; chr17:g.39727407G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727407G>C , CM000679.2:g.39727407G>C	GRCh38
NC_000017.10:g.37883660G>C , CM000679.1:g.37883660G>C	GRCh37
NC_000017.9:g.35137186G>C	NCBI36
NG_007503.1:g.44268G>C , LRG_724:g.44268G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3272G>C MANE Select	ENSP00000269571.4:p.Gly1091Ala
ENST00000269571.9:c.3272G>C	ENSP00000269571.4:p.Gly1091Ala
ENST00000406381.6:c.3182G>C	ENSP00000385185.2:p.Gly1061Ala
ENST00000445658.6:c.2444G>C	ENSP00000404047.2:p.Gly815Ala
ENST00000541774.5:c.3227G>C	ENSP00000446466.1:p.Gly1076Ala
ENST00000578373.5:c.*3062G>C	ENSP00000463427.1:n.*3062G>C
ENST00000584450.5:c.3160-282G>C	ENSP00000463714.1:n.3160-282G>C
ENST00000584601.5:c.3182G>C	ENSP00000462438.1:p.Gly1061Ala
NM_001005862.2:c.3182G>C , LRG_724t1:c.3182G>C	NP_001005862.1:p.Gly1061Ala
NM_001289936.1:c.3227G>C , LRG_724t4:c.3227G>C	NP_001276865.1:p.Gly1076Ala
NM_001289937.1:c.3160-282G>C	NP_001276866.1:n.3160-282G>C
NM_004448.3:c.3272G>C , LRG_724t2:c.3272G>C	NP_004439.2:p.Gly1091Ala
NR_110535.1:n.3596G>C
XM_024450641.1:c.3410G>C	XP_024306409.1:p.Gly1137Ala
XM_024450642.1:c.3365G>C	XP_024306410.1:p.Gly1122Ala
XM_024450643.1:c.3320G>C	XP_024306411.1:p.Gly1107Ala
NM_001005862.3:c.3182G>C	NP_001005862.1:p.Gly1061Ala
NM_001289936.2:c.3227G>C	NP_001276865.1:p.Gly1076Ala
NM_001289937.2:c.3160-282G>C	NP_001276866.1:n.3160-282G>C
NM_001382782.1:c.3182G>C	NP_001369711.1:p.Gly1061Ala
NM_001382783.1:c.3182G>C	NP_001369712.1:p.Gly1061Ala
NM_001382784.1:c.3389G>C	NP_001369713.1:p.Gly1130Ala
NM_001382785.1:c.3374G>C	NP_001369714.1:p.Gly1125Ala
NM_001382786.1:c.3353G>C	NP_001369715.1:p.Gly1118Ala
NM_001382787.1:c.3347G>C	NP_001369716.1:p.Gly1116Ala
NM_001382788.1:c.3302G>C	NP_001369717.1:p.Gly1101Ala
NM_001382789.1:c.3293G>C	NP_001369718.1:p.Gly1098Ala
NM_001382790.1:c.3269G>C	NP_001369719.1:p.Gly1090Ala
NM_001382791.1:c.3263G>C	NP_001369720.1:p.Gly1088Ala
NM_001382792.1:c.3236G>C	NP_001369721.1:p.Gly1079Ala
NM_001382793.1:c.3230G>C	NP_001369722.1:p.Gly1077Ala
NM_001382794.1:c.3230G>C	NP_001369723.1:p.Gly1077Ala
NM_001382795.1:c.3224G>C	NP_001369724.1:p.Gly1075Ala
NM_001382796.1:c.3185G>C	NP_001369725.1:p.Gly1062Ala
NM_001382797.1:c.3173G>C	NP_001369726.1:p.Gly1058Ala
NM_001382798.1:c.3116G>C	NP_001369727.1:p.Gly1039Ala
NM_001382799.1:c.3092G>C	NP_001369728.1:p.Gly1031Ala
NM_001382800.1:c.3086G>C	NP_001369729.1:p.Gly1029Ala
NM_001382801.1:c.3068G>C	NP_001369730.1:p.Gly1023Ala
NM_001382802.1:c.3014G>C	NP_001369731.1:p.Gly1005Ala
NM_001382803.1:c.3118-282G>C	NP_001369732.1:n.3118-282G>C
NM_001382804.1:c.2444G>C	NP_001369733.1:p.Gly815Ala
NM_001382805.1:c.2321G>C	NP_001369734.1:p.Gly774Ala
NM_001382806.1:c.2234G>C	NP_001369735.1:p.Gly745Ala
NM_004448.4:c.3272G>C MANE Select	NP_004439.2:p.Gly1091Ala
NR_110535.2:n.3510G>C