Canonical Allele Identifier: CA499890239

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143250944
• MyVariant Identifiers: chr17:g.37883712T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727459T>A , CM000679.2:g.39727459T>A	GRCh38
NC_000017.10:g.37883712T>A , CM000679.1:g.37883712T>A	GRCh37
NC_000017.9:g.35137238T>A	NCBI36
NG_007503.1:g.44320T>A , LRG_724:g.44320T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3324T>A MANE Select	ENSP00000269571.4:p.Pro1108=
ENST00000269571.9:c.3324T>A	ENSP00000269571.4:p.Pro1108=
ENST00000406381.6:c.3234T>A	ENSP00000385185.2:p.Pro1078=
ENST00000445658.6:c.2496T>A	ENSP00000404047.2:p.Pro832=
ENST00000541774.5:c.3279T>A	ENSP00000446466.1:p.Pro1093=
ENST00000578373.5:c.*3114T>A	ENSP00000463427.1:n.*3114T>A
ENST00000584450.5:c.3160-230T>A	ENSP00000463714.1:n.3160-230T>A
ENST00000584601.5:c.3234T>A	ENSP00000462438.1:p.Pro1078=
NM_001005862.2:c.3234T>A , LRG_724t1:c.3234T>A	NP_001005862.1:p.Pro1078=
NM_001289936.1:c.3279T>A , LRG_724t4:c.3279T>A	NP_001276865.1:p.Pro1093=
NM_001289937.1:c.3160-230T>A	NP_001276866.1:n.3160-230T>A
NM_004448.3:c.3324T>A , LRG_724t2:c.3324T>A	NP_004439.2:p.Pro1108=
NR_110535.1:n.3648T>A
XM_024450641.1:c.3462T>A	XP_024306409.1:p.Pro1154=
XM_024450642.1:c.3417T>A	XP_024306410.1:p.Pro1139=
XM_024450643.1:c.3372T>A	XP_024306411.1:p.Pro1124=
NM_001005862.3:c.3234T>A	NP_001005862.1:p.Pro1078=
NM_001289936.2:c.3279T>A	NP_001276865.1:p.Pro1093=
NM_001289937.2:c.3160-230T>A	NP_001276866.1:n.3160-230T>A
NM_001382782.1:c.3234T>A	NP_001369711.1:p.Pro1078=
NM_001382783.1:c.3234T>A	NP_001369712.1:p.Pro1078=
NM_001382784.1:c.3441T>A	NP_001369713.1:p.Pro1147=
NM_001382785.1:c.3426T>A	NP_001369714.1:p.Pro1142=
NM_001382786.1:c.3405T>A	NP_001369715.1:p.Pro1135=
NM_001382787.1:c.3399T>A	NP_001369716.1:p.Pro1133=
NM_001382788.1:c.3354T>A	NP_001369717.1:p.Pro1118=
NM_001382789.1:c.3345T>A	NP_001369718.1:p.Pro1115=
NM_001382790.1:c.3321T>A	NP_001369719.1:p.Pro1107=
NM_001382791.1:c.3315T>A	NP_001369720.1:p.Pro1105=
NM_001382792.1:c.3288T>A	NP_001369721.1:p.Pro1096=
NM_001382793.1:c.3282T>A	NP_001369722.1:p.Pro1094=
NM_001382794.1:c.3282T>A	NP_001369723.1:p.Pro1094=
NM_001382795.1:c.3276T>A	NP_001369724.1:p.Pro1092=
NM_001382796.1:c.3237T>A	NP_001369725.1:p.Pro1079=
NM_001382797.1:c.3225T>A	NP_001369726.1:p.Pro1075=
NM_001382798.1:c.3168T>A	NP_001369727.1:p.Pro1056=
NM_001382799.1:c.3144T>A	NP_001369728.1:p.Pro1048=
NM_001382800.1:c.3138T>A	NP_001369729.1:p.Pro1046=
NM_001382801.1:c.3120T>A	NP_001369730.1:p.Pro1040=
NM_001382802.1:c.3066T>A	NP_001369731.1:p.Pro1022=
NM_001382803.1:c.3118-230T>A	NP_001369732.1:n.3118-230T>A
NM_001382804.1:c.2496T>A	NP_001369733.1:p.Pro832=
NM_001382805.1:c.2373T>A	NP_001369734.1:p.Pro791=
NM_001382806.1:c.2286T>A	NP_001369735.1:p.Pro762=
NM_004448.4:c.3324T>A MANE Select	NP_004439.2:p.Pro1108=
NR_110535.2:n.3562T>A