Canonical Allele Identifier: CA399313340

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37884056G>C (hg19) ; chr17:g.39727803G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727803G>C , CM000679.2:g.39727803G>C	GRCh38
NC_000017.10:g.37884056G>C , CM000679.1:g.37884056G>C	GRCh37
NC_000017.9:g.35137582G>C	NCBI36
NG_007503.1:g.44664G>C , LRG_724:g.44664G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3527G>C MANE Select	ENSP00000269571.4:p.Gly1176Ala
ENST00000269571.9:c.3527G>C	ENSP00000269571.4:p.Gly1176Ala
ENST00000406381.6:c.3437G>C	ENSP00000385185.2:p.Gly1146Ala
ENST00000445658.6:c.2699G>C	ENSP00000404047.2:p.Gly900Ala
ENST00000541774.5:c.3482G>C	ENSP00000446466.1:p.Gly1161Ala
ENST00000578373.5:c.*3317G>C	ENSP00000463427.1:n.*3317G>C
ENST00000584450.5:c.*106G>C	ENSP00000463714.1:n.*106G>C
ENST00000584601.5:c.3437G>C	ENSP00000462438.1:p.Gly1146Ala
NM_001005862.2:c.3437G>C , LRG_724t1:c.3437G>C	NP_001005862.1:p.Gly1146Ala
NM_001289936.1:c.3482G>C , LRG_724t4:c.3482G>C	NP_001276865.1:p.Gly1161Ala
NM_001289937.1:c.*106G>C	NP_001276866.1:n.*106G>C
NM_004448.3:c.3527G>C , LRG_724t2:c.3527G>C	NP_004439.2:p.Gly1176Ala
NR_110535.1:n.3851G>C
XM_024450641.1:c.3665G>C	XP_024306409.1:p.Gly1222Ala
XM_024450642.1:c.3620G>C	XP_024306410.1:p.Gly1207Ala
XM_024450643.1:c.3575G>C	XP_024306411.1:p.Gly1192Ala
NM_001005862.3:c.3437G>C	NP_001005862.1:p.Gly1146Ala
NM_001289936.2:c.3482G>C	NP_001276865.1:p.Gly1161Ala
NM_001289937.2:c.*106G>C	NP_001276866.1:n.*106G>C
NM_001382782.1:c.3437G>C	NP_001369711.1:p.Gly1146Ala
NM_001382783.1:c.3437G>C	NP_001369712.1:p.Gly1146Ala
NM_001382784.1:c.3644G>C	NP_001369713.1:p.Gly1215Ala
NM_001382785.1:c.3629G>C	NP_001369714.1:p.Gly1210Ala
NM_001382786.1:c.3608G>C	NP_001369715.1:p.Gly1203Ala
NM_001382787.1:c.3602G>C	NP_001369716.1:p.Gly1201Ala
NM_001382788.1:c.3557G>C	NP_001369717.1:p.Gly1186Ala
NM_001382789.1:c.3548G>C	NP_001369718.1:p.Gly1183Ala
NM_001382790.1:c.3524G>C	NP_001369719.1:p.Gly1175Ala
NM_001382791.1:c.3518G>C	NP_001369720.1:p.Gly1173Ala
NM_001382792.1:c.3491G>C	NP_001369721.1:p.Gly1164Ala
NM_001382793.1:c.3485G>C	NP_001369722.1:p.Gly1162Ala
NM_001382794.1:c.3485G>C	NP_001369723.1:p.Gly1162Ala
NM_001382795.1:c.3479G>C	NP_001369724.1:p.Gly1160Ala
NM_001382796.1:c.3440G>C	NP_001369725.1:p.Gly1147Ala
NM_001382797.1:c.3428G>C	NP_001369726.1:p.Gly1143Ala
NM_001382798.1:c.3371G>C	NP_001369727.1:p.Gly1124Ala
NM_001382799.1:c.3347G>C	NP_001369728.1:p.Gly1116Ala
NM_001382800.1:c.3341G>C	NP_001369729.1:p.Gly1114Ala
NM_001382801.1:c.3323G>C	NP_001369730.1:p.Gly1108Ala
NM_001382802.1:c.3269G>C	NP_001369731.1:p.Gly1090Ala
NM_001382803.1:c.*106G>C	NP_001369732.1:n.*106G>C
NM_001382804.1:c.2699G>C	NP_001369733.1:p.Gly900Ala
NM_001382805.1:c.2576G>C	NP_001369734.1:p.Gly859Ala
NM_001382806.1:c.2489G>C	NP_001369735.1:p.Gly830Ala
NM_004448.4:c.3527G>C MANE Select	NP_004439.2:p.Gly1176Ala
NR_110535.2:n.3765G>C