Canonical Allele Identifier: CA399314306

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37884184A>T (hg19) ; chr17:g.39727931A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727931A>T , CM000679.2:g.39727931A>T	GRCh38
NC_000017.10:g.37884184A>T , CM000679.1:g.37884184A>T	GRCh37
NC_000017.9:g.35137710A>T	NCBI36
NG_007503.1:g.44792A>T , LRG_724:g.44792A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3655A>T MANE Select	ENSP00000269571.4:p.Asn1219Tyr
ENST00000269571.9:c.3655A>T	ENSP00000269571.4:p.Asn1219Tyr
ENST00000406381.6:c.3565A>T	ENSP00000385185.2:p.Asn1189Tyr
ENST00000445658.6:c.2827A>T	ENSP00000404047.2:p.Asn943Tyr
ENST00000541774.5:c.3610A>T	ENSP00000446466.1:p.Asn1204Tyr
ENST00000578373.5:c.*3445A>T	ENSP00000463427.1:n.*3445A>T
ENST00000584450.5:c.*234A>T	ENSP00000463714.1:n.*234A>T
ENST00000584601.5:c.3565A>T	ENSP00000462438.1:p.Asn1189Tyr
NM_001005862.2:c.3565A>T , LRG_724t1:c.3565A>T	NP_001005862.1:p.Asn1189Tyr
NM_001289936.1:c.3610A>T , LRG_724t4:c.3610A>T	NP_001276865.1:p.Asn1204Tyr
NM_001289937.1:c.*234A>T	NP_001276866.1:n.*234A>T
NM_004448.3:c.3655A>T , LRG_724t2:c.3655A>T	NP_004439.2:p.Asn1219Tyr
NR_110535.1:n.3979A>T
XM_024450641.1:c.3793A>T	XP_024306409.1:p.Asn1265Tyr
XM_024450642.1:c.3748A>T	XP_024306410.1:p.Asn1250Tyr
XM_024450643.1:c.3703A>T	XP_024306411.1:p.Asn1235Tyr
NM_001005862.3:c.3565A>T	NP_001005862.1:p.Asn1189Tyr
NM_001289936.2:c.3610A>T	NP_001276865.1:p.Asn1204Tyr
NM_001289937.2:c.*234A>T	NP_001276866.1:n.*234A>T
NM_001382782.1:c.3565A>T	NP_001369711.1:p.Asn1189Tyr
NM_001382783.1:c.3565A>T	NP_001369712.1:p.Asn1189Tyr
NM_001382784.1:c.3772A>T	NP_001369713.1:p.Asn1258Tyr
NM_001382785.1:c.3757A>T	NP_001369714.1:p.Asn1253Tyr
NM_001382786.1:c.3736A>T	NP_001369715.1:p.Asn1246Tyr
NM_001382787.1:c.3730A>T	NP_001369716.1:p.Asn1244Tyr
NM_001382788.1:c.3685A>T	NP_001369717.1:p.Asn1229Tyr
NM_001382789.1:c.3676A>T	NP_001369718.1:p.Asn1226Tyr
NM_001382790.1:c.3652A>T	NP_001369719.1:p.Asn1218Tyr
NM_001382791.1:c.3646A>T	NP_001369720.1:p.Asn1216Tyr
NM_001382792.1:c.3619A>T	NP_001369721.1:p.Asn1207Tyr
NM_001382793.1:c.3613A>T	NP_001369722.1:p.Asn1205Tyr
NM_001382794.1:c.3613A>T	NP_001369723.1:p.Asn1205Tyr
NM_001382795.1:c.3607A>T	NP_001369724.1:p.Asn1203Tyr
NM_001382796.1:c.3568A>T	NP_001369725.1:p.Asn1190Tyr
NM_001382797.1:c.3556A>T	NP_001369726.1:p.Asn1186Tyr
NM_001382798.1:c.3499A>T	NP_001369727.1:p.Asn1167Tyr
NM_001382799.1:c.3475A>T	NP_001369728.1:p.Asn1159Tyr
NM_001382800.1:c.3469A>T	NP_001369729.1:p.Asn1157Tyr
NM_001382801.1:c.3451A>T	NP_001369730.1:p.Asn1151Tyr
NM_001382802.1:c.3397A>T	NP_001369731.1:p.Asn1133Tyr
NM_001382803.1:c.*234A>T	NP_001369732.1:n.*234A>T
NM_001382804.1:c.2827A>T	NP_001369733.1:p.Asn943Tyr
NM_001382805.1:c.2704A>T	NP_001369734.1:p.Asn902Tyr
NM_001382806.1:c.2617A>T	NP_001369735.1:p.Asn873Tyr
NM_004448.4:c.3655A>T MANE Select	NP_004439.2:p.Asn1219Tyr
NR_110535.2:n.3893A>T