Canonical Allele Identifier: CA399314504

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143314337
• MyVariant Identifiers: chr17:g.37884208C>G (hg19) ; chr17:g.39727955C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727955C>G , CM000679.2:g.39727955C>G	GRCh38
NC_000017.10:g.37884208C>G , CM000679.1:g.37884208C>G	GRCh37
NC_000017.9:g.35137734C>G	NCBI36
NG_007503.1:g.44816C>G , LRG_724:g.44816C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3679C>G MANE Select	ENSP00000269571.4:p.Pro1227Ala
ENST00000269571.9:c.3679C>G	ENSP00000269571.4:p.Pro1227Ala
ENST00000406381.6:c.3589C>G	ENSP00000385185.2:p.Pro1197Ala
ENST00000445658.6:c.2851C>G	ENSP00000404047.2:p.Pro951Ala
ENST00000541774.5:c.3634C>G	ENSP00000446466.1:p.Pro1212Ala
ENST00000578373.5:c.*3469C>G	ENSP00000463427.1:n.*3469C>G
ENST00000584450.5:c.*258C>G	ENSP00000463714.1:n.*258C>G
ENST00000584601.5:c.3589C>G	ENSP00000462438.1:p.Pro1197Ala
NM_001005862.2:c.3589C>G , LRG_724t1:c.3589C>G	NP_001005862.1:p.Pro1197Ala
NM_001289936.1:c.3634C>G , LRG_724t4:c.3634C>G	NP_001276865.1:p.Pro1212Ala
NM_001289937.1:c.*258C>G	NP_001276866.1:n.*258C>G
NM_004448.3:c.3679C>G , LRG_724t2:c.3679C>G	NP_004439.2:p.Pro1227Ala
NR_110535.1:n.4003C>G
XM_024450641.1:c.3817C>G	XP_024306409.1:p.Pro1273Ala
XM_024450642.1:c.3772C>G	XP_024306410.1:p.Pro1258Ala
XM_024450643.1:c.3727C>G	XP_024306411.1:p.Pro1243Ala
NM_001005862.3:c.3589C>G	NP_001005862.1:p.Pro1197Ala
NM_001289936.2:c.3634C>G	NP_001276865.1:p.Pro1212Ala
NM_001289937.2:c.*258C>G	NP_001276866.1:n.*258C>G
NM_001382782.1:c.3589C>G	NP_001369711.1:p.Pro1197Ala
NM_001382783.1:c.3589C>G	NP_001369712.1:p.Pro1197Ala
NM_001382784.1:c.3796C>G	NP_001369713.1:p.Pro1266Ala
NM_001382785.1:c.3781C>G	NP_001369714.1:p.Pro1261Ala
NM_001382786.1:c.3760C>G	NP_001369715.1:p.Pro1254Ala
NM_001382787.1:c.3754C>G	NP_001369716.1:p.Pro1252Ala
NM_001382788.1:c.3709C>G	NP_001369717.1:p.Pro1237Ala
NM_001382789.1:c.3700C>G	NP_001369718.1:p.Pro1234Ala
NM_001382790.1:c.3676C>G	NP_001369719.1:p.Pro1226Ala
NM_001382791.1:c.3670C>G	NP_001369720.1:p.Pro1224Ala
NM_001382792.1:c.3643C>G	NP_001369721.1:p.Pro1215Ala
NM_001382793.1:c.3637C>G	NP_001369722.1:p.Pro1213Ala
NM_001382794.1:c.3637C>G	NP_001369723.1:p.Pro1213Ala
NM_001382795.1:c.3631C>G	NP_001369724.1:p.Pro1211Ala
NM_001382796.1:c.3592C>G	NP_001369725.1:p.Pro1198Ala
NM_001382797.1:c.3580C>G	NP_001369726.1:p.Pro1194Ala
NM_001382798.1:c.3523C>G	NP_001369727.1:p.Pro1175Ala
NM_001382799.1:c.3499C>G	NP_001369728.1:p.Pro1167Ala
NM_001382800.1:c.3493C>G	NP_001369729.1:p.Pro1165Ala
NM_001382801.1:c.3475C>G	NP_001369730.1:p.Pro1159Ala
NM_001382802.1:c.3421C>G	NP_001369731.1:p.Pro1141Ala
NM_001382803.1:c.*258C>G	NP_001369732.1:n.*258C>G
NM_001382804.1:c.2851C>G	NP_001369733.1:p.Pro951Ala
NM_001382805.1:c.2728C>G	NP_001369734.1:p.Pro910Ala
NM_001382806.1:c.2641C>G	NP_001369735.1:p.Pro881Ala
NM_004448.4:c.3679C>G MANE Select	NP_004439.2:p.Pro1227Ala
NR_110535.2:n.3917C>G