Canonical Allele Identifier: CA399313558

Gene: ERBB2

Linked Data

• dbSNP Id: rs1597892828
• MyVariant Identifiers: chr17:g.37884085G>T (hg19) ; chr17:g.39727832G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727832G>T , CM000679.2:g.39727832G>T	GRCh38
NC_000017.10:g.37884085G>T , CM000679.1:g.37884085G>T	GRCh37
NC_000017.9:g.35137611G>T	NCBI36
NG_007503.1:g.44693G>T , LRG_724:g.44693G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3556G>T MANE Select	ENSP00000269571.4:p.Ala1186Ser
ENST00000269571.9:c.3556G>T	ENSP00000269571.4:p.Ala1186Ser
ENST00000406381.6:c.3466G>T	ENSP00000385185.2:p.Ala1156Ser
ENST00000445658.6:c.2728G>T	ENSP00000404047.2:p.Ala910Ser
ENST00000541774.5:c.3511G>T	ENSP00000446466.1:p.Ala1171Ser
ENST00000578373.5:c.*3346G>T	ENSP00000463427.1:n.*3346G>T
ENST00000584450.5:c.*135G>T	ENSP00000463714.1:n.*135G>T
ENST00000584601.5:c.3466G>T	ENSP00000462438.1:p.Ala1156Ser
NM_001005862.2:c.3466G>T , LRG_724t1:c.3466G>T	NP_001005862.1:p.Ala1156Ser
NM_001289936.1:c.3511G>T , LRG_724t4:c.3511G>T	NP_001276865.1:p.Ala1171Ser
NM_001289937.1:c.*135G>T	NP_001276866.1:n.*135G>T
NM_004448.3:c.3556G>T , LRG_724t2:c.3556G>T	NP_004439.2:p.Ala1186Ser
NR_110535.1:n.3880G>T
XM_024450641.1:c.3694G>T	XP_024306409.1:p.Ala1232Ser
XM_024450642.1:c.3649G>T	XP_024306410.1:p.Ala1217Ser
XM_024450643.1:c.3604G>T	XP_024306411.1:p.Ala1202Ser
NM_001005862.3:c.3466G>T	NP_001005862.1:p.Ala1156Ser
NM_001289936.2:c.3511G>T	NP_001276865.1:p.Ala1171Ser
NM_001289937.2:c.*135G>T	NP_001276866.1:n.*135G>T
NM_001382782.1:c.3466G>T	NP_001369711.1:p.Ala1156Ser
NM_001382783.1:c.3466G>T	NP_001369712.1:p.Ala1156Ser
NM_001382784.1:c.3673G>T	NP_001369713.1:p.Ala1225Ser
NM_001382785.1:c.3658G>T	NP_001369714.1:p.Ala1220Ser
NM_001382786.1:c.3637G>T	NP_001369715.1:p.Ala1213Ser
NM_001382787.1:c.3631G>T	NP_001369716.1:p.Ala1211Ser
NM_001382788.1:c.3586G>T	NP_001369717.1:p.Ala1196Ser
NM_001382789.1:c.3577G>T	NP_001369718.1:p.Ala1193Ser
NM_001382790.1:c.3553G>T	NP_001369719.1:p.Ala1185Ser
NM_001382791.1:c.3547G>T	NP_001369720.1:p.Ala1183Ser
NM_001382792.1:c.3520G>T	NP_001369721.1:p.Ala1174Ser
NM_001382793.1:c.3514G>T	NP_001369722.1:p.Ala1172Ser
NM_001382794.1:c.3514G>T	NP_001369723.1:p.Ala1172Ser
NM_001382795.1:c.3508G>T	NP_001369724.1:p.Ala1170Ser
NM_001382796.1:c.3469G>T	NP_001369725.1:p.Ala1157Ser
NM_001382797.1:c.3457G>T	NP_001369726.1:p.Ala1153Ser
NM_001382798.1:c.3400G>T	NP_001369727.1:p.Ala1134Ser
NM_001382799.1:c.3376G>T	NP_001369728.1:p.Ala1126Ser
NM_001382800.1:c.3370G>T	NP_001369729.1:p.Ala1124Ser
NM_001382801.1:c.3352G>T	NP_001369730.1:p.Ala1118Ser
NM_001382802.1:c.3298G>T	NP_001369731.1:p.Ala1100Ser
NM_001382803.1:c.*135G>T	NP_001369732.1:n.*135G>T
NM_001382804.1:c.2728G>T	NP_001369733.1:p.Ala910Ser
NM_001382805.1:c.2605G>T	NP_001369734.1:p.Ala869Ser
NM_001382806.1:c.2518G>T	NP_001369735.1:p.Ala840Ser
NM_004448.4:c.3556G>T MANE Select	NP_004439.2:p.Ala1186Ser
NR_110535.2:n.3794G>T