Canonical Allele Identifier: CA399314126

Gene: ERBB2

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3632C>A MANE Select	ENSP00000269571.4:p.Pro1211His
ENST00000269571.9:c.3632C>A	ENSP00000269571.4:p.Pro1211His
ENST00000406381.6:c.3542C>A	ENSP00000385185.2:p.Pro1181His
ENST00000445658.6:c.2804C>A	ENSP00000404047.2:p.Pro935His
ENST00000541774.5:c.3587C>A	ENSP00000446466.1:p.Pro1196His
ENST00000578373.5:c.*3422C>A	ENSP00000463427.1:n.*3422C>A
ENST00000584450.5:c.*211C>A	ENSP00000463714.1:n.*211C>A
ENST00000584601.5:c.3542C>A	ENSP00000462438.1:p.Pro1181His
NM_001005862.2:c.3542C>A , LRG_724t1:c.3542C>A	NP_001005862.1:p.Pro1181His
NM_001289936.1:c.3587C>A , LRG_724t4:c.3587C>A	NP_001276865.1:p.Pro1196His
NM_001289937.1:c.*211C>A	NP_001276866.1:n.*211C>A
NM_004448.3:c.3632C>A , LRG_724t2:c.3632C>A	NP_004439.2:p.Pro1211His
NR_110535.1:n.3956C>A
XM_024450641.1:c.3770C>A	XP_024306409.1:p.Pro1257His
XM_024450642.1:c.3725C>A	XP_024306410.1:p.Pro1242His
XM_024450643.1:c.3680C>A	XP_024306411.1:p.Pro1227His
NM_001005862.3:c.3542C>A	NP_001005862.1:p.Pro1181His
NM_001289936.2:c.3587C>A	NP_001276865.1:p.Pro1196His
NM_001289937.2:c.*211C>A	NP_001276866.1:n.*211C>A
NM_001382782.1:c.3542C>A	NP_001369711.1:p.Pro1181His
NM_001382783.1:c.3542C>A	NP_001369712.1:p.Pro1181His
NM_001382784.1:c.3749C>A	NP_001369713.1:p.Pro1250His
NM_001382785.1:c.3734C>A	NP_001369714.1:p.Pro1245His
NM_001382786.1:c.3713C>A	NP_001369715.1:p.Pro1238His
NM_001382787.1:c.3707C>A	NP_001369716.1:p.Pro1236His
NM_001382788.1:c.3662C>A	NP_001369717.1:p.Pro1221His
NM_001382789.1:c.3653C>A	NP_001369718.1:p.Pro1218His
NM_001382790.1:c.3629C>A	NP_001369719.1:p.Pro1210His
NM_001382791.1:c.3623C>A	NP_001369720.1:p.Pro1208His
NM_001382792.1:c.3596C>A	NP_001369721.1:p.Pro1199His
NM_001382793.1:c.3590C>A	NP_001369722.1:p.Pro1197His
NM_001382794.1:c.3590C>A	NP_001369723.1:p.Pro1197His
NM_001382795.1:c.3584C>A	NP_001369724.1:p.Pro1195His
NM_001382796.1:c.3545C>A	NP_001369725.1:p.Pro1182His
NM_001382797.1:c.3533C>A	NP_001369726.1:p.Pro1178His
NM_001382798.1:c.3476C>A	NP_001369727.1:p.Pro1159His
NM_001382799.1:c.3452C>A	NP_001369728.1:p.Pro1151His
NM_001382800.1:c.3446C>A	NP_001369729.1:p.Pro1149His
NM_001382801.1:c.3428C>A	NP_001369730.1:p.Pro1143His
NM_001382802.1:c.3374C>A	NP_001369731.1:p.Pro1125His
NM_001382803.1:c.*211C>A	NP_001369732.1:n.*211C>A
NM_001382804.1:c.2804C>A	NP_001369733.1:p.Pro935His
NM_001382805.1:c.2681C>A	NP_001369734.1:p.Pro894His
NM_001382806.1:c.2594C>A	NP_001369735.1:p.Pro865His
NM_004448.4:c.3632C>A MANE Select	NP_004439.2:p.Pro1211His
NR_110535.2:n.3870C>A