Canonical Allele Identifier: CA399314127

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143310231
• MyVariant Identifiers: chr17:g.37884161C>G (hg19) ; chr17:g.39727908C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727908C>G , CM000679.2:g.39727908C>G	GRCh38
NC_000017.10:g.37884161C>G , CM000679.1:g.37884161C>G	GRCh37
NC_000017.9:g.35137687C>G	NCBI36
NG_007503.1:g.44769C>G , LRG_724:g.44769C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3632C>G MANE Select	ENSP00000269571.4:p.Pro1211Arg
ENST00000269571.9:c.3632C>G	ENSP00000269571.4:p.Pro1211Arg
ENST00000406381.6:c.3542C>G	ENSP00000385185.2:p.Pro1181Arg
ENST00000445658.6:c.2804C>G	ENSP00000404047.2:p.Pro935Arg
ENST00000541774.5:c.3587C>G	ENSP00000446466.1:p.Pro1196Arg
ENST00000578373.5:c.*3422C>G	ENSP00000463427.1:n.*3422C>G
ENST00000584450.5:c.*211C>G	ENSP00000463714.1:n.*211C>G
ENST00000584601.5:c.3542C>G	ENSP00000462438.1:p.Pro1181Arg
NM_001005862.2:c.3542C>G , LRG_724t1:c.3542C>G	NP_001005862.1:p.Pro1181Arg
NM_001289936.1:c.3587C>G , LRG_724t4:c.3587C>G	NP_001276865.1:p.Pro1196Arg
NM_001289937.1:c.*211C>G	NP_001276866.1:n.*211C>G
NM_004448.3:c.3632C>G , LRG_724t2:c.3632C>G	NP_004439.2:p.Pro1211Arg
NR_110535.1:n.3956C>G
XM_024450641.1:c.3770C>G	XP_024306409.1:p.Pro1257Arg
XM_024450642.1:c.3725C>G	XP_024306410.1:p.Pro1242Arg
XM_024450643.1:c.3680C>G	XP_024306411.1:p.Pro1227Arg
NM_001005862.3:c.3542C>G	NP_001005862.1:p.Pro1181Arg
NM_001289936.2:c.3587C>G	NP_001276865.1:p.Pro1196Arg
NM_001289937.2:c.*211C>G	NP_001276866.1:n.*211C>G
NM_001382782.1:c.3542C>G	NP_001369711.1:p.Pro1181Arg
NM_001382783.1:c.3542C>G	NP_001369712.1:p.Pro1181Arg
NM_001382784.1:c.3749C>G	NP_001369713.1:p.Pro1250Arg
NM_001382785.1:c.3734C>G	NP_001369714.1:p.Pro1245Arg
NM_001382786.1:c.3713C>G	NP_001369715.1:p.Pro1238Arg
NM_001382787.1:c.3707C>G	NP_001369716.1:p.Pro1236Arg
NM_001382788.1:c.3662C>G	NP_001369717.1:p.Pro1221Arg
NM_001382789.1:c.3653C>G	NP_001369718.1:p.Pro1218Arg
NM_001382790.1:c.3629C>G	NP_001369719.1:p.Pro1210Arg
NM_001382791.1:c.3623C>G	NP_001369720.1:p.Pro1208Arg
NM_001382792.1:c.3596C>G	NP_001369721.1:p.Pro1199Arg
NM_001382793.1:c.3590C>G	NP_001369722.1:p.Pro1197Arg
NM_001382794.1:c.3590C>G	NP_001369723.1:p.Pro1197Arg
NM_001382795.1:c.3584C>G	NP_001369724.1:p.Pro1195Arg
NM_001382796.1:c.3545C>G	NP_001369725.1:p.Pro1182Arg
NM_001382797.1:c.3533C>G	NP_001369726.1:p.Pro1178Arg
NM_001382798.1:c.3476C>G	NP_001369727.1:p.Pro1159Arg
NM_001382799.1:c.3452C>G	NP_001369728.1:p.Pro1151Arg
NM_001382800.1:c.3446C>G	NP_001369729.1:p.Pro1149Arg
NM_001382801.1:c.3428C>G	NP_001369730.1:p.Pro1143Arg
NM_001382802.1:c.3374C>G	NP_001369731.1:p.Pro1125Arg
NM_001382803.1:c.*211C>G	NP_001369732.1:n.*211C>G
NM_001382804.1:c.2804C>G	NP_001369733.1:p.Pro935Arg
NM_001382805.1:c.2681C>G	NP_001369734.1:p.Pro894Arg
NM_001382806.1:c.2594C>G	NP_001369735.1:p.Pro865Arg
NM_004448.4:c.3632C>G MANE Select	NP_004439.2:p.Pro1211Arg
NR_110535.2:n.3870C>G