Canonical Allele Identifier: CA399312644

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143254298
• MyVariant Identifiers: chr17:g.37883743C>T (hg19) ; chr17:g.39727490C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727490C>T , CM000679.2:g.39727490C>T	GRCh38
NC_000017.10:g.37883743C>T , CM000679.1:g.37883743C>T	GRCh37
NC_000017.9:g.35137269C>T	NCBI36
NG_007503.1:g.44351C>T , LRG_724:g.44351C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3355C>T MANE Select	ENSP00000269571.4:p.Pro1119Ser
ENST00000269571.9:c.3355C>T	ENSP00000269571.4:p.Pro1119Ser
ENST00000406381.6:c.3265C>T	ENSP00000385185.2:p.Pro1089Ser
ENST00000445658.6:c.2527C>T	ENSP00000404047.2:p.Pro843Ser
ENST00000541774.5:c.3310C>T	ENSP00000446466.1:p.Pro1104Ser
ENST00000578373.5:c.*3145C>T	ENSP00000463427.1:n.*3145C>T
ENST00000584450.5:c.3160-199C>T	ENSP00000463714.1:n.3160-199C>T
ENST00000584601.5:c.3265C>T	ENSP00000462438.1:p.Pro1089Ser
NM_001005862.2:c.3265C>T , LRG_724t1:c.3265C>T	NP_001005862.1:p.Pro1089Ser
NM_001289936.1:c.3310C>T , LRG_724t4:c.3310C>T	NP_001276865.1:p.Pro1104Ser
NM_001289937.1:c.3160-199C>T	NP_001276866.1:n.3160-199C>T
NM_004448.3:c.3355C>T , LRG_724t2:c.3355C>T	NP_004439.2:p.Pro1119Ser
NR_110535.1:n.3679C>T
XM_024450641.1:c.3493C>T	XP_024306409.1:p.Pro1165Ser
XM_024450642.1:c.3448C>T	XP_024306410.1:p.Pro1150Ser
XM_024450643.1:c.3403C>T	XP_024306411.1:p.Pro1135Ser
NM_001005862.3:c.3265C>T	NP_001005862.1:p.Pro1089Ser
NM_001289936.2:c.3310C>T	NP_001276865.1:p.Pro1104Ser
NM_001289937.2:c.3160-199C>T	NP_001276866.1:n.3160-199C>T
NM_001382782.1:c.3265C>T	NP_001369711.1:p.Pro1089Ser
NM_001382783.1:c.3265C>T	NP_001369712.1:p.Pro1089Ser
NM_001382784.1:c.3472C>T	NP_001369713.1:p.Pro1158Ser
NM_001382785.1:c.3457C>T	NP_001369714.1:p.Pro1153Ser
NM_001382786.1:c.3436C>T	NP_001369715.1:p.Pro1146Ser
NM_001382787.1:c.3430C>T	NP_001369716.1:p.Pro1144Ser
NM_001382788.1:c.3385C>T	NP_001369717.1:p.Pro1129Ser
NM_001382789.1:c.3376C>T	NP_001369718.1:p.Pro1126Ser
NM_001382790.1:c.3352C>T	NP_001369719.1:p.Pro1118Ser
NM_001382791.1:c.3346C>T	NP_001369720.1:p.Pro1116Ser
NM_001382792.1:c.3319C>T	NP_001369721.1:p.Pro1107Ser
NM_001382793.1:c.3313C>T	NP_001369722.1:p.Pro1105Ser
NM_001382794.1:c.3313C>T	NP_001369723.1:p.Pro1105Ser
NM_001382795.1:c.3307C>T	NP_001369724.1:p.Pro1103Ser
NM_001382796.1:c.3268C>T	NP_001369725.1:p.Pro1090Ser
NM_001382797.1:c.3256C>T	NP_001369726.1:p.Pro1086Ser
NM_001382798.1:c.3199C>T	NP_001369727.1:p.Pro1067Ser
NM_001382799.1:c.3175C>T	NP_001369728.1:p.Pro1059Ser
NM_001382800.1:c.3169C>T	NP_001369729.1:p.Pro1057Ser
NM_001382801.1:c.3151C>T	NP_001369730.1:p.Pro1051Ser
NM_001382802.1:c.3097C>T	NP_001369731.1:p.Pro1033Ser
NM_001382803.1:c.3118-199C>T	NP_001369732.1:n.3118-199C>T
NM_001382804.1:c.2527C>T	NP_001369733.1:p.Pro843Ser
NM_001382805.1:c.2404C>T	NP_001369734.1:p.Pro802Ser
NM_001382806.1:c.2317C>T	NP_001369735.1:p.Pro773Ser
NM_004448.4:c.3355C>T MANE Select	NP_004439.2:p.Pro1119Ser
NR_110535.2:n.3593C>T