Canonical Allele Identifier: CA399314036

Gene: ERBB2

Linked Data

• dbSNP Id: rs145772320
• MyVariant Identifiers: chr17:g.37884149C>G (hg19) ; chr17:g.39727896C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727896C>G , CM000679.2:g.39727896C>G	GRCh38
NC_000017.10:g.37884149C>G , CM000679.1:g.37884149C>G	GRCh37
NC_000017.9:g.35137675C>G	NCBI36
NG_007503.1:g.44757C>G , LRG_724:g.44757C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3620C>G MANE Select	ENSP00000269571.4:p.Pro1207Arg
ENST00000269571.9:c.3620C>G	ENSP00000269571.4:p.Pro1207Arg
ENST00000406381.6:c.3530C>G	ENSP00000385185.2:p.Pro1177Arg
ENST00000445658.6:c.2792C>G	ENSP00000404047.2:p.Pro931Arg
ENST00000541774.5:c.3575C>G	ENSP00000446466.1:p.Pro1192Arg
ENST00000578373.5:c.*3410C>G	ENSP00000463427.1:n.*3410C>G
ENST00000584450.5:c.*199C>G	ENSP00000463714.1:n.*199C>G
ENST00000584601.5:c.3530C>G	ENSP00000462438.1:p.Pro1177Arg
NM_001005862.2:c.3530C>G , LRG_724t1:c.3530C>G	NP_001005862.1:p.Pro1177Arg
NM_001289936.1:c.3575C>G , LRG_724t4:c.3575C>G	NP_001276865.1:p.Pro1192Arg
NM_001289937.1:c.*199C>G	NP_001276866.1:n.*199C>G
NM_004448.3:c.3620C>G , LRG_724t2:c.3620C>G	NP_004439.2:p.Pro1207Arg
NR_110535.1:n.3944C>G
XM_024450641.1:c.3758C>G	XP_024306409.1:p.Pro1253Arg
XM_024450642.1:c.3713C>G	XP_024306410.1:p.Pro1238Arg
XM_024450643.1:c.3668C>G	XP_024306411.1:p.Pro1223Arg
NM_001005862.3:c.3530C>G	NP_001005862.1:p.Pro1177Arg
NM_001289936.2:c.3575C>G	NP_001276865.1:p.Pro1192Arg
NM_001289937.2:c.*199C>G	NP_001276866.1:n.*199C>G
NM_001382782.1:c.3530C>G	NP_001369711.1:p.Pro1177Arg
NM_001382783.1:c.3530C>G	NP_001369712.1:p.Pro1177Arg
NM_001382784.1:c.3737C>G	NP_001369713.1:p.Pro1246Arg
NM_001382785.1:c.3722C>G	NP_001369714.1:p.Pro1241Arg
NM_001382786.1:c.3701C>G	NP_001369715.1:p.Pro1234Arg
NM_001382787.1:c.3695C>G	NP_001369716.1:p.Pro1232Arg
NM_001382788.1:c.3650C>G	NP_001369717.1:p.Pro1217Arg
NM_001382789.1:c.3641C>G	NP_001369718.1:p.Pro1214Arg
NM_001382790.1:c.3617C>G	NP_001369719.1:p.Pro1206Arg
NM_001382791.1:c.3611C>G	NP_001369720.1:p.Pro1204Arg
NM_001382792.1:c.3584C>G	NP_001369721.1:p.Pro1195Arg
NM_001382793.1:c.3578C>G	NP_001369722.1:p.Pro1193Arg
NM_001382794.1:c.3578C>G	NP_001369723.1:p.Pro1193Arg
NM_001382795.1:c.3572C>G	NP_001369724.1:p.Pro1191Arg
NM_001382796.1:c.3533C>G	NP_001369725.1:p.Pro1178Arg
NM_001382797.1:c.3521C>G	NP_001369726.1:p.Pro1174Arg
NM_001382798.1:c.3464C>G	NP_001369727.1:p.Pro1155Arg
NM_001382799.1:c.3440C>G	NP_001369728.1:p.Pro1147Arg
NM_001382800.1:c.3434C>G	NP_001369729.1:p.Pro1145Arg
NM_001382801.1:c.3416C>G	NP_001369730.1:p.Pro1139Arg
NM_001382802.1:c.3362C>G	NP_001369731.1:p.Pro1121Arg
NM_001382803.1:c.*199C>G	NP_001369732.1:n.*199C>G
NM_001382804.1:c.2792C>G	NP_001369733.1:p.Pro931Arg
NM_001382805.1:c.2669C>G	NP_001369734.1:p.Pro890Arg
NM_001382806.1:c.2582C>G	NP_001369735.1:p.Pro861Arg
NM_004448.4:c.3620C>G MANE Select	NP_004439.2:p.Pro1207Arg
NR_110535.2:n.3858C>G