Canonical Allele Identifier: CA499890289

Gene: ERBB2

Linked Data

• dbSNP Id: rs771812007
• MyVariant Identifiers: chr17:g.37883778C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727525C>A , CM000679.2:g.39727525C>A	GRCh38
NC_000017.10:g.37883778C>A , CM000679.1:g.37883778C>A	GRCh37
NC_000017.9:g.35137304C>A	NCBI36
NG_007503.1:g.44386C>A , LRG_724:g.44386C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3390C>A MANE Select	ENSP00000269571.4:p.Pro1130=
ENST00000269571.9:c.3390C>A	ENSP00000269571.4:p.Pro1130=
ENST00000406381.6:c.3300C>A	ENSP00000385185.2:p.Pro1100=
ENST00000445658.6:c.2562C>A	ENSP00000404047.2:p.Pro854=
ENST00000541774.5:c.3345C>A	ENSP00000446466.1:p.Pro1115=
ENST00000578373.5:c.*3180C>A	ENSP00000463427.1:n.*3180C>A
ENST00000584450.5:c.3160-164C>A	ENSP00000463714.1:n.3160-164C>A
ENST00000584601.5:c.3300C>A	ENSP00000462438.1:p.Pro1100=
NM_001005862.2:c.3300C>A , LRG_724t1:c.3300C>A	NP_001005862.1:p.Pro1100=
NM_001289936.1:c.3345C>A , LRG_724t4:c.3345C>A	NP_001276865.1:p.Pro1115=
NM_001289937.1:c.3160-164C>A	NP_001276866.1:n.3160-164C>A
NM_004448.3:c.3390C>A , LRG_724t2:c.3390C>A	NP_004439.2:p.Pro1130=
NR_110535.1:n.3714C>A
XM_024450641.1:c.3528C>A	XP_024306409.1:p.Pro1176=
XM_024450642.1:c.3483C>A	XP_024306410.1:p.Pro1161=
XM_024450643.1:c.3438C>A	XP_024306411.1:p.Pro1146=
NM_001005862.3:c.3300C>A	NP_001005862.1:p.Pro1100=
NM_001289936.2:c.3345C>A	NP_001276865.1:p.Pro1115=
NM_001289937.2:c.3160-164C>A	NP_001276866.1:n.3160-164C>A
NM_001382782.1:c.3300C>A	NP_001369711.1:p.Pro1100=
NM_001382783.1:c.3300C>A	NP_001369712.1:p.Pro1100=
NM_001382784.1:c.3507C>A	NP_001369713.1:p.Pro1169=
NM_001382785.1:c.3492C>A	NP_001369714.1:p.Pro1164=
NM_001382786.1:c.3471C>A	NP_001369715.1:p.Pro1157=
NM_001382787.1:c.3465C>A	NP_001369716.1:p.Pro1155=
NM_001382788.1:c.3420C>A	NP_001369717.1:p.Pro1140=
NM_001382789.1:c.3411C>A	NP_001369718.1:p.Pro1137=
NM_001382790.1:c.3387C>A	NP_001369719.1:p.Pro1129=
NM_001382791.1:c.3381C>A	NP_001369720.1:p.Pro1127=
NM_001382792.1:c.3354C>A	NP_001369721.1:p.Pro1118=
NM_001382793.1:c.3348C>A	NP_001369722.1:p.Pro1116=
NM_001382794.1:c.3348C>A	NP_001369723.1:p.Pro1116=
NM_001382795.1:c.3342C>A	NP_001369724.1:p.Pro1114=
NM_001382796.1:c.3303C>A	NP_001369725.1:p.Pro1101=
NM_001382797.1:c.3291C>A	NP_001369726.1:p.Pro1097=
NM_001382798.1:c.3234C>A	NP_001369727.1:p.Pro1078=
NM_001382799.1:c.3210C>A	NP_001369728.1:p.Pro1070=
NM_001382800.1:c.3204C>A	NP_001369729.1:p.Pro1068=
NM_001382801.1:c.3186C>A	NP_001369730.1:p.Pro1062=
NM_001382802.1:c.3132C>A	NP_001369731.1:p.Pro1044=
NM_001382803.1:c.3118-164C>A	NP_001369732.1:n.3118-164C>A
NM_001382804.1:c.2562C>A	NP_001369733.1:p.Pro854=
NM_001382805.1:c.2439C>A	NP_001369734.1:p.Pro813=
NM_001382806.1:c.2352C>A	NP_001369735.1:p.Pro784=
NM_004448.4:c.3390C>A MANE Select	NP_004439.2:p.Pro1130=
NR_110535.2:n.3628C>A