Canonical Allele Identifier: CA399313209

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143296369
• MyVariant Identifiers: chr17:g.37884038C>G (hg19) ; chr17:g.39727785C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727785C>G , CM000679.2:g.39727785C>G	GRCh38
NC_000017.10:g.37884038C>G , CM000679.1:g.37884038C>G	GRCh37
NC_000017.9:g.35137564C>G	NCBI36
NG_007503.1:g.44646C>G , LRG_724:g.44646C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3509C>G MANE Select	ENSP00000269571.4:p.Pro1170Arg
ENST00000269571.9:c.3509C>G	ENSP00000269571.4:p.Pro1170Arg
ENST00000406381.6:c.3419C>G	ENSP00000385185.2:p.Pro1140Arg
ENST00000445658.6:c.2681C>G	ENSP00000404047.2:p.Pro894Arg
ENST00000541774.5:c.3464C>G	ENSP00000446466.1:p.Pro1155Arg
ENST00000578373.5:c.*3299C>G	ENSP00000463427.1:n.*3299C>G
ENST00000584450.5:c.*88C>G	ENSP00000463714.1:n.*88C>G
ENST00000584601.5:c.3419C>G	ENSP00000462438.1:p.Pro1140Arg
NM_001005862.2:c.3419C>G , LRG_724t1:c.3419C>G	NP_001005862.1:p.Pro1140Arg
NM_001289936.1:c.3464C>G , LRG_724t4:c.3464C>G	NP_001276865.1:p.Pro1155Arg
NM_001289937.1:c.*88C>G	NP_001276866.1:n.*88C>G
NM_004448.3:c.3509C>G , LRG_724t2:c.3509C>G	NP_004439.2:p.Pro1170Arg
NR_110535.1:n.3833C>G
XM_024450641.1:c.3647C>G	XP_024306409.1:p.Pro1216Arg
XM_024450642.1:c.3602C>G	XP_024306410.1:p.Pro1201Arg
XM_024450643.1:c.3557C>G	XP_024306411.1:p.Pro1186Arg
NM_001005862.3:c.3419C>G	NP_001005862.1:p.Pro1140Arg
NM_001289936.2:c.3464C>G	NP_001276865.1:p.Pro1155Arg
NM_001289937.2:c.*88C>G	NP_001276866.1:n.*88C>G
NM_001382782.1:c.3419C>G	NP_001369711.1:p.Pro1140Arg
NM_001382783.1:c.3419C>G	NP_001369712.1:p.Pro1140Arg
NM_001382784.1:c.3626C>G	NP_001369713.1:p.Pro1209Arg
NM_001382785.1:c.3611C>G	NP_001369714.1:p.Pro1204Arg
NM_001382786.1:c.3590C>G	NP_001369715.1:p.Pro1197Arg
NM_001382787.1:c.3584C>G	NP_001369716.1:p.Pro1195Arg
NM_001382788.1:c.3539C>G	NP_001369717.1:p.Pro1180Arg
NM_001382789.1:c.3530C>G	NP_001369718.1:p.Pro1177Arg
NM_001382790.1:c.3506C>G	NP_001369719.1:p.Pro1169Arg
NM_001382791.1:c.3500C>G	NP_001369720.1:p.Pro1167Arg
NM_001382792.1:c.3473C>G	NP_001369721.1:p.Pro1158Arg
NM_001382793.1:c.3467C>G	NP_001369722.1:p.Pro1156Arg
NM_001382794.1:c.3467C>G	NP_001369723.1:p.Pro1156Arg
NM_001382795.1:c.3461C>G	NP_001369724.1:p.Pro1154Arg
NM_001382796.1:c.3422C>G	NP_001369725.1:p.Pro1141Arg
NM_001382797.1:c.3410C>G	NP_001369726.1:p.Pro1137Arg
NM_001382798.1:c.3353C>G	NP_001369727.1:p.Pro1118Arg
NM_001382799.1:c.3329C>G	NP_001369728.1:p.Pro1110Arg
NM_001382800.1:c.3323C>G	NP_001369729.1:p.Pro1108Arg
NM_001382801.1:c.3305C>G	NP_001369730.1:p.Pro1102Arg
NM_001382802.1:c.3251C>G	NP_001369731.1:p.Pro1084Arg
NM_001382803.1:c.*88C>G	NP_001369732.1:n.*88C>G
NM_001382804.1:c.2681C>G	NP_001369733.1:p.Pro894Arg
NM_001382805.1:c.2558C>G	NP_001369734.1:p.Pro853Arg
NM_001382806.1:c.2471C>G	NP_001369735.1:p.Pro824Arg
NM_004448.4:c.3509C>G MANE Select	NP_004439.2:p.Pro1170Arg
NR_110535.2:n.3747C>G