Canonical Allele Identifier: CA399310901

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37883693C>G (hg19) ; chr17:g.39727440C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727440C>G , CM000679.2:g.39727440C>G	GRCh38
NC_000017.10:g.37883693C>G , CM000679.1:g.37883693C>G	GRCh37
NC_000017.9:g.35137219C>G	NCBI36
NG_007503.1:g.44301C>G , LRG_724:g.44301C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3305C>G MANE Select	ENSP00000269571.4:p.Pro1102Arg
ENST00000269571.9:c.3305C>G	ENSP00000269571.4:p.Pro1102Arg
ENST00000406381.6:c.3215C>G	ENSP00000385185.2:p.Pro1072Arg
ENST00000445658.6:c.2477C>G	ENSP00000404047.2:p.Pro826Arg
ENST00000541774.5:c.3260C>G	ENSP00000446466.1:p.Pro1087Arg
ENST00000578373.5:c.*3095C>G	ENSP00000463427.1:n.*3095C>G
ENST00000584450.5:c.3160-249C>G	ENSP00000463714.1:n.3160-249C>G
ENST00000584601.5:c.3215C>G	ENSP00000462438.1:p.Pro1072Arg
NM_001005862.2:c.3215C>G , LRG_724t1:c.3215C>G	NP_001005862.1:p.Pro1072Arg
NM_001289936.1:c.3260C>G , LRG_724t4:c.3260C>G	NP_001276865.1:p.Pro1087Arg
NM_001289937.1:c.3160-249C>G	NP_001276866.1:n.3160-249C>G
NM_004448.3:c.3305C>G , LRG_724t2:c.3305C>G	NP_004439.2:p.Pro1102Arg
NR_110535.1:n.3629C>G
XM_024450641.1:c.3443C>G	XP_024306409.1:p.Pro1148Arg
XM_024450642.1:c.3398C>G	XP_024306410.1:p.Pro1133Arg
XM_024450643.1:c.3353C>G	XP_024306411.1:p.Pro1118Arg
NM_001005862.3:c.3215C>G	NP_001005862.1:p.Pro1072Arg
NM_001289936.2:c.3260C>G	NP_001276865.1:p.Pro1087Arg
NM_001289937.2:c.3160-249C>G	NP_001276866.1:n.3160-249C>G
NM_001382782.1:c.3215C>G	NP_001369711.1:p.Pro1072Arg
NM_001382783.1:c.3215C>G	NP_001369712.1:p.Pro1072Arg
NM_001382784.1:c.3422C>G	NP_001369713.1:p.Pro1141Arg
NM_001382785.1:c.3407C>G	NP_001369714.1:p.Pro1136Arg
NM_001382786.1:c.3386C>G	NP_001369715.1:p.Pro1129Arg
NM_001382787.1:c.3380C>G	NP_001369716.1:p.Pro1127Arg
NM_001382788.1:c.3335C>G	NP_001369717.1:p.Pro1112Arg
NM_001382789.1:c.3326C>G	NP_001369718.1:p.Pro1109Arg
NM_001382790.1:c.3302C>G	NP_001369719.1:p.Pro1101Arg
NM_001382791.1:c.3296C>G	NP_001369720.1:p.Pro1099Arg
NM_001382792.1:c.3269C>G	NP_001369721.1:p.Pro1090Arg
NM_001382793.1:c.3263C>G	NP_001369722.1:p.Pro1088Arg
NM_001382794.1:c.3263C>G	NP_001369723.1:p.Pro1088Arg
NM_001382795.1:c.3257C>G	NP_001369724.1:p.Pro1086Arg
NM_001382796.1:c.3218C>G	NP_001369725.1:p.Pro1073Arg
NM_001382797.1:c.3206C>G	NP_001369726.1:p.Pro1069Arg
NM_001382798.1:c.3149C>G	NP_001369727.1:p.Pro1050Arg
NM_001382799.1:c.3125C>G	NP_001369728.1:p.Pro1042Arg
NM_001382800.1:c.3119C>G	NP_001369729.1:p.Pro1040Arg
NM_001382801.1:c.3101C>G	NP_001369730.1:p.Pro1034Arg
NM_001382802.1:c.3047C>G	NP_001369731.1:p.Pro1016Arg
NM_001382803.1:c.3118-249C>G	NP_001369732.1:n.3118-249C>G
NM_001382804.1:c.2477C>G	NP_001369733.1:p.Pro826Arg
NM_001382805.1:c.2354C>G	NP_001369734.1:p.Pro785Arg
NM_001382806.1:c.2267C>G	NP_001369735.1:p.Pro756Arg
NM_004448.4:c.3305C>G MANE Select	NP_004439.2:p.Pro1102Arg
NR_110535.2:n.3543C>G