Canonical Allele Identifier: CA399313297

Gene: ERBB2

Linked Data

• dbSNP Id: rs1351450168
• MyVariant Identifiers: chr17:g.37884050C>A (hg19) ; chr17:g.39727797C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727797C>A , CM000679.2:g.39727797C>A	GRCh38
NC_000017.10:g.37884050C>A , CM000679.1:g.37884050C>A	GRCh37
NC_000017.9:g.35137576C>A	NCBI36
NG_007503.1:g.44658C>A , LRG_724:g.44658C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3521C>A MANE Select	ENSP00000269571.4:p.Ser1174Tyr
ENST00000269571.9:c.3521C>A	ENSP00000269571.4:p.Ser1174Tyr
ENST00000406381.6:c.3431C>A	ENSP00000385185.2:p.Ser1144Tyr
ENST00000445658.6:c.2693C>A	ENSP00000404047.2:p.Ser898Tyr
ENST00000541774.5:c.3476C>A	ENSP00000446466.1:p.Ser1159Tyr
ENST00000578373.5:c.*3311C>A	ENSP00000463427.1:n.*3311C>A
ENST00000584450.5:c.*100C>A	ENSP00000463714.1:n.*100C>A
ENST00000584601.5:c.3431C>A	ENSP00000462438.1:p.Ser1144Tyr
NM_001005862.2:c.3431C>A , LRG_724t1:c.3431C>A	NP_001005862.1:p.Ser1144Tyr
NM_001289936.1:c.3476C>A , LRG_724t4:c.3476C>A	NP_001276865.1:p.Ser1159Tyr
NM_001289937.1:c.*100C>A	NP_001276866.1:n.*100C>A
NM_004448.3:c.3521C>A , LRG_724t2:c.3521C>A	NP_004439.2:p.Ser1174Tyr
NR_110535.1:n.3845C>A
XM_024450641.1:c.3659C>A	XP_024306409.1:p.Ser1220Tyr
XM_024450642.1:c.3614C>A	XP_024306410.1:p.Ser1205Tyr
XM_024450643.1:c.3569C>A	XP_024306411.1:p.Ser1190Tyr
NM_001005862.3:c.3431C>A	NP_001005862.1:p.Ser1144Tyr
NM_001289936.2:c.3476C>A	NP_001276865.1:p.Ser1159Tyr
NM_001289937.2:c.*100C>A	NP_001276866.1:n.*100C>A
NM_001382782.1:c.3431C>A	NP_001369711.1:p.Ser1144Tyr
NM_001382783.1:c.3431C>A	NP_001369712.1:p.Ser1144Tyr
NM_001382784.1:c.3638C>A	NP_001369713.1:p.Ser1213Tyr
NM_001382785.1:c.3623C>A	NP_001369714.1:p.Ser1208Tyr
NM_001382786.1:c.3602C>A	NP_001369715.1:p.Ser1201Tyr
NM_001382787.1:c.3596C>A	NP_001369716.1:p.Ser1199Tyr
NM_001382788.1:c.3551C>A	NP_001369717.1:p.Ser1184Tyr
NM_001382789.1:c.3542C>A	NP_001369718.1:p.Ser1181Tyr
NM_001382790.1:c.3518C>A	NP_001369719.1:p.Ser1173Tyr
NM_001382791.1:c.3512C>A	NP_001369720.1:p.Ser1171Tyr
NM_001382792.1:c.3485C>A	NP_001369721.1:p.Ser1162Tyr
NM_001382793.1:c.3479C>A	NP_001369722.1:p.Ser1160Tyr
NM_001382794.1:c.3479C>A	NP_001369723.1:p.Ser1160Tyr
NM_001382795.1:c.3473C>A	NP_001369724.1:p.Ser1158Tyr
NM_001382796.1:c.3434C>A	NP_001369725.1:p.Ser1145Tyr
NM_001382797.1:c.3422C>A	NP_001369726.1:p.Ser1141Tyr
NM_001382798.1:c.3365C>A	NP_001369727.1:p.Ser1122Tyr
NM_001382799.1:c.3341C>A	NP_001369728.1:p.Ser1114Tyr
NM_001382800.1:c.3335C>A	NP_001369729.1:p.Ser1112Tyr
NM_001382801.1:c.3317C>A	NP_001369730.1:p.Ser1106Tyr
NM_001382802.1:c.3263C>A	NP_001369731.1:p.Ser1088Tyr
NM_001382803.1:c.*100C>A	NP_001369732.1:n.*100C>A
NM_001382804.1:c.2693C>A	NP_001369733.1:p.Ser898Tyr
NM_001382805.1:c.2570C>A	NP_001369734.1:p.Ser857Tyr
NM_001382806.1:c.2483C>A	NP_001369735.1:p.Ser828Tyr
NM_004448.4:c.3521C>A MANE Select	NP_004439.2:p.Ser1174Tyr
NR_110535.2:n.3759C>A