Canonical Allele Identifier: CA399312889

Gene: ERBB2

Linked Data

• dbSNP Id: rs2059857710
• gnomAD v4: 17-39727721-C-T
• MyVariant Identifiers: chr17:g.37883974C>T (hg19) ; chr17:g.39727721C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727721C>T , CM000679.2:g.39727721C>T	GRCh38
NC_000017.10:g.37883974C>T , CM000679.1:g.37883974C>T	GRCh37
NC_000017.9:g.35137500C>T	NCBI36
NG_007503.1:g.44582C>T , LRG_724:g.44582C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3445C>T MANE Select	ENSP00000269571.4:p.Pro1149Ser
ENST00000269571.9:c.3445C>T	ENSP00000269571.4:p.Pro1149Ser
ENST00000406381.6:c.3355C>T	ENSP00000385185.2:p.Pro1119Ser
ENST00000445658.6:c.2617C>T	ENSP00000404047.2:p.Pro873Ser
ENST00000541774.5:c.3400C>T	ENSP00000446466.1:p.Pro1134Ser
ENST00000578373.5:c.*3235C>T	ENSP00000463427.1:n.*3235C>T
ENST00000584450.5:c.*24C>T	ENSP00000463714.1:n.*24C>T
ENST00000584601.5:c.3355C>T	ENSP00000462438.1:p.Pro1119Ser
NM_001005862.2:c.3355C>T , LRG_724t1:c.3355C>T	NP_001005862.1:p.Pro1119Ser
NM_001289936.1:c.3400C>T , LRG_724t4:c.3400C>T	NP_001276865.1:p.Pro1134Ser
NM_001289937.1:c.*24C>T	NP_001276866.1:n.*24C>T
NM_004448.3:c.3445C>T , LRG_724t2:c.3445C>T	NP_004439.2:p.Pro1149Ser
NR_110535.1:n.3769C>T
XM_024450641.1:c.3583C>T	XP_024306409.1:p.Pro1195Ser
XM_024450642.1:c.3538C>T	XP_024306410.1:p.Pro1180Ser
XM_024450643.1:c.3493C>T	XP_024306411.1:p.Pro1165Ser
NM_001005862.3:c.3355C>T	NP_001005862.1:p.Pro1119Ser
NM_001289936.2:c.3400C>T	NP_001276865.1:p.Pro1134Ser
NM_001289937.2:c.*24C>T	NP_001276866.1:n.*24C>T
NM_001382782.1:c.3355C>T	NP_001369711.1:p.Pro1119Ser
NM_001382783.1:c.3355C>T	NP_001369712.1:p.Pro1119Ser
NM_001382784.1:c.3562C>T	NP_001369713.1:p.Pro1188Ser
NM_001382785.1:c.3547C>T	NP_001369714.1:p.Pro1183Ser
NM_001382786.1:c.3526C>T	NP_001369715.1:p.Pro1176Ser
NM_001382787.1:c.3520C>T	NP_001369716.1:p.Pro1174Ser
NM_001382788.1:c.3475C>T	NP_001369717.1:p.Pro1159Ser
NM_001382789.1:c.3466C>T	NP_001369718.1:p.Pro1156Ser
NM_001382790.1:c.3442C>T	NP_001369719.1:p.Pro1148Ser
NM_001382791.1:c.3436C>T	NP_001369720.1:p.Pro1146Ser
NM_001382792.1:c.3409C>T	NP_001369721.1:p.Pro1137Ser
NM_001382793.1:c.3403C>T	NP_001369722.1:p.Pro1135Ser
NM_001382794.1:c.3403C>T	NP_001369723.1:p.Pro1135Ser
NM_001382795.1:c.3397C>T	NP_001369724.1:p.Pro1133Ser
NM_001382796.1:c.3358C>T	NP_001369725.1:p.Pro1120Ser
NM_001382797.1:c.3346C>T	NP_001369726.1:p.Pro1116Ser
NM_001382798.1:c.3289C>T	NP_001369727.1:p.Pro1097Ser
NM_001382799.1:c.3265C>T	NP_001369728.1:p.Pro1089Ser
NM_001382800.1:c.3259C>T	NP_001369729.1:p.Pro1087Ser
NM_001382801.1:c.3241C>T	NP_001369730.1:p.Pro1081Ser
NM_001382802.1:c.3187C>T	NP_001369731.1:p.Pro1063Ser
NM_001382803.1:c.*24C>T	NP_001369732.1:n.*24C>T
NM_001382804.1:c.2617C>T	NP_001369733.1:p.Pro873Ser
NM_001382805.1:c.2494C>T	NP_001369734.1:p.Pro832Ser
NM_001382806.1:c.2407C>T	NP_001369735.1:p.Pro803Ser
NM_004448.4:c.3445C>T MANE Select	NP_004439.2:p.Pro1149Ser
NR_110535.2:n.3683C>T