Canonical Allele Identifier: CA399313304

Gene: ERBB2

Linked Data

• dbSNP Id: rs1437065997
• MyVariant Identifiers: chr17:g.37884052C>A (hg19) ; chr17:g.39727799C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727799C>A , CM000679.2:g.39727799C>A	GRCh38
NC_000017.10:g.37884052C>A , CM000679.1:g.37884052C>A	GRCh37
NC_000017.9:g.35137578C>A	NCBI36
NG_007503.1:g.44660C>A , LRG_724:g.44660C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3523C>A MANE Select	ENSP00000269571.4:p.Pro1175Thr
ENST00000269571.9:c.3523C>A	ENSP00000269571.4:p.Pro1175Thr
ENST00000406381.6:c.3433C>A	ENSP00000385185.2:p.Pro1145Thr
ENST00000445658.6:c.2695C>A	ENSP00000404047.2:p.Pro899Thr
ENST00000541774.5:c.3478C>A	ENSP00000446466.1:p.Pro1160Thr
ENST00000578373.5:c.*3313C>A	ENSP00000463427.1:n.*3313C>A
ENST00000584450.5:c.*102C>A	ENSP00000463714.1:n.*102C>A
ENST00000584601.5:c.3433C>A	ENSP00000462438.1:p.Pro1145Thr
NM_001005862.2:c.3433C>A , LRG_724t1:c.3433C>A	NP_001005862.1:p.Pro1145Thr
NM_001289936.1:c.3478C>A , LRG_724t4:c.3478C>A	NP_001276865.1:p.Pro1160Thr
NM_001289937.1:c.*102C>A	NP_001276866.1:n.*102C>A
NM_004448.3:c.3523C>A , LRG_724t2:c.3523C>A	NP_004439.2:p.Pro1175Thr
NR_110535.1:n.3847C>A
XM_024450641.1:c.3661C>A	XP_024306409.1:p.Pro1221Thr
XM_024450642.1:c.3616C>A	XP_024306410.1:p.Pro1206Thr
XM_024450643.1:c.3571C>A	XP_024306411.1:p.Pro1191Thr
NM_001005862.3:c.3433C>A	NP_001005862.1:p.Pro1145Thr
NM_001289936.2:c.3478C>A	NP_001276865.1:p.Pro1160Thr
NM_001289937.2:c.*102C>A	NP_001276866.1:n.*102C>A
NM_001382782.1:c.3433C>A	NP_001369711.1:p.Pro1145Thr
NM_001382783.1:c.3433C>A	NP_001369712.1:p.Pro1145Thr
NM_001382784.1:c.3640C>A	NP_001369713.1:p.Pro1214Thr
NM_001382785.1:c.3625C>A	NP_001369714.1:p.Pro1209Thr
NM_001382786.1:c.3604C>A	NP_001369715.1:p.Pro1202Thr
NM_001382787.1:c.3598C>A	NP_001369716.1:p.Pro1200Thr
NM_001382788.1:c.3553C>A	NP_001369717.1:p.Pro1185Thr
NM_001382789.1:c.3544C>A	NP_001369718.1:p.Pro1182Thr
NM_001382790.1:c.3520C>A	NP_001369719.1:p.Pro1174Thr
NM_001382791.1:c.3514C>A	NP_001369720.1:p.Pro1172Thr
NM_001382792.1:c.3487C>A	NP_001369721.1:p.Pro1163Thr
NM_001382793.1:c.3481C>A	NP_001369722.1:p.Pro1161Thr
NM_001382794.1:c.3481C>A	NP_001369723.1:p.Pro1161Thr
NM_001382795.1:c.3475C>A	NP_001369724.1:p.Pro1159Thr
NM_001382796.1:c.3436C>A	NP_001369725.1:p.Pro1146Thr
NM_001382797.1:c.3424C>A	NP_001369726.1:p.Pro1142Thr
NM_001382798.1:c.3367C>A	NP_001369727.1:p.Pro1123Thr
NM_001382799.1:c.3343C>A	NP_001369728.1:p.Pro1115Thr
NM_001382800.1:c.3337C>A	NP_001369729.1:p.Pro1113Thr
NM_001382801.1:c.3319C>A	NP_001369730.1:p.Pro1107Thr
NM_001382802.1:c.3265C>A	NP_001369731.1:p.Pro1089Thr
NM_001382803.1:c.*102C>A	NP_001369732.1:n.*102C>A
NM_001382804.1:c.2695C>A	NP_001369733.1:p.Pro899Thr
NM_001382805.1:c.2572C>A	NP_001369734.1:p.Pro858Thr
NM_001382806.1:c.2485C>A	NP_001369735.1:p.Pro829Thr
NM_004448.4:c.3523C>A MANE Select	NP_004439.2:p.Pro1175Thr
NR_110535.2:n.3761C>A