Canonical Allele Identifier: CA399312749

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143258145
• gnomAD v4: 17-39727521-C-T
• MyVariant Identifiers: chr17:g.37883774C>T (hg19) ; chr17:g.39727521C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727521C>T , CM000679.2:g.39727521C>T	GRCh38
NC_000017.10:g.37883774C>T , CM000679.1:g.37883774C>T	GRCh37
NC_000017.9:g.35137300C>T	NCBI36
NG_007503.1:g.44382C>T , LRG_724:g.44382C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3386C>T MANE Select	ENSP00000269571.4:p.Ala1129Val
ENST00000269571.9:c.3386C>T	ENSP00000269571.4:p.Ala1129Val
ENST00000406381.6:c.3296C>T	ENSP00000385185.2:p.Ala1099Val
ENST00000445658.6:c.2558C>T	ENSP00000404047.2:p.Ala853Val
ENST00000541774.5:c.3341C>T	ENSP00000446466.1:p.Ala1114Val
ENST00000578373.5:c.*3176C>T	ENSP00000463427.1:n.*3176C>T
ENST00000584450.5:c.3160-168C>T	ENSP00000463714.1:n.3160-168C>T
ENST00000584601.5:c.3296C>T	ENSP00000462438.1:p.Ala1099Val
NM_001005862.2:c.3296C>T , LRG_724t1:c.3296C>T	NP_001005862.1:p.Ala1099Val
NM_001289936.1:c.3341C>T , LRG_724t4:c.3341C>T	NP_001276865.1:p.Ala1114Val
NM_001289937.1:c.3160-168C>T	NP_001276866.1:n.3160-168C>T
NM_004448.3:c.3386C>T , LRG_724t2:c.3386C>T	NP_004439.2:p.Ala1129Val
NR_110535.1:n.3710C>T
XM_024450641.1:c.3524C>T	XP_024306409.1:p.Ala1175Val
XM_024450642.1:c.3479C>T	XP_024306410.1:p.Ala1160Val
XM_024450643.1:c.3434C>T	XP_024306411.1:p.Ala1145Val
NM_001005862.3:c.3296C>T	NP_001005862.1:p.Ala1099Val
NM_001289936.2:c.3341C>T	NP_001276865.1:p.Ala1114Val
NM_001289937.2:c.3160-168C>T	NP_001276866.1:n.3160-168C>T
NM_001382782.1:c.3296C>T	NP_001369711.1:p.Ala1099Val
NM_001382783.1:c.3296C>T	NP_001369712.1:p.Ala1099Val
NM_001382784.1:c.3503C>T	NP_001369713.1:p.Ala1168Val
NM_001382785.1:c.3488C>T	NP_001369714.1:p.Ala1163Val
NM_001382786.1:c.3467C>T	NP_001369715.1:p.Ala1156Val
NM_001382787.1:c.3461C>T	NP_001369716.1:p.Ala1154Val
NM_001382788.1:c.3416C>T	NP_001369717.1:p.Ala1139Val
NM_001382789.1:c.3407C>T	NP_001369718.1:p.Ala1136Val
NM_001382790.1:c.3383C>T	NP_001369719.1:p.Ala1128Val
NM_001382791.1:c.3377C>T	NP_001369720.1:p.Ala1126Val
NM_001382792.1:c.3350C>T	NP_001369721.1:p.Ala1117Val
NM_001382793.1:c.3344C>T	NP_001369722.1:p.Ala1115Val
NM_001382794.1:c.3344C>T	NP_001369723.1:p.Ala1115Val
NM_001382795.1:c.3338C>T	NP_001369724.1:p.Ala1113Val
NM_001382796.1:c.3299C>T	NP_001369725.1:p.Ala1100Val
NM_001382797.1:c.3287C>T	NP_001369726.1:p.Ala1096Val
NM_001382798.1:c.3230C>T	NP_001369727.1:p.Ala1077Val
NM_001382799.1:c.3206C>T	NP_001369728.1:p.Ala1069Val
NM_001382800.1:c.3200C>T	NP_001369729.1:p.Ala1067Val
NM_001382801.1:c.3182C>T	NP_001369730.1:p.Ala1061Val
NM_001382802.1:c.3128C>T	NP_001369731.1:p.Ala1043Val
NM_001382803.1:c.3118-168C>T	NP_001369732.1:n.3118-168C>T
NM_001382804.1:c.2558C>T	NP_001369733.1:p.Ala853Val
NM_001382805.1:c.2435C>T	NP_001369734.1:p.Ala812Val
NM_001382806.1:c.2348C>T	NP_001369735.1:p.Ala783Val
NM_004448.4:c.3386C>T MANE Select	NP_004439.2:p.Ala1129Val
NR_110535.2:n.3624C>T