Canonical Allele Identifier: CA399312934

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143291840
• MyVariant Identifiers: chr17:g.37883995C>A (hg19) ; chr17:g.39727742C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727742C>A , CM000679.2:g.39727742C>A	GRCh38
NC_000017.10:g.37883995C>A , CM000679.1:g.37883995C>A	GRCh37
NC_000017.9:g.35137521C>A	NCBI36
NG_007503.1:g.44603C>A , LRG_724:g.44603C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3466C>A MANE Select	ENSP00000269571.4:p.Pro1156Thr
ENST00000269571.9:c.3466C>A	ENSP00000269571.4:p.Pro1156Thr
ENST00000406381.6:c.3376C>A	ENSP00000385185.2:p.Pro1126Thr
ENST00000445658.6:c.2638C>A	ENSP00000404047.2:p.Pro880Thr
ENST00000541774.5:c.3421C>A	ENSP00000446466.1:p.Pro1141Thr
ENST00000578373.5:c.*3256C>A	ENSP00000463427.1:n.*3256C>A
ENST00000584450.5:c.*45C>A	ENSP00000463714.1:n.*45C>A
ENST00000584601.5:c.3376C>A	ENSP00000462438.1:p.Pro1126Thr
NM_001005862.2:c.3376C>A , LRG_724t1:c.3376C>A	NP_001005862.1:p.Pro1126Thr
NM_001289936.1:c.3421C>A , LRG_724t4:c.3421C>A	NP_001276865.1:p.Pro1141Thr
NM_001289937.1:c.*45C>A	NP_001276866.1:n.*45C>A
NM_004448.3:c.3466C>A , LRG_724t2:c.3466C>A	NP_004439.2:p.Pro1156Thr
NR_110535.1:n.3790C>A
XM_024450641.1:c.3604C>A	XP_024306409.1:p.Pro1202Thr
XM_024450642.1:c.3559C>A	XP_024306410.1:p.Pro1187Thr
XM_024450643.1:c.3514C>A	XP_024306411.1:p.Pro1172Thr
NM_001005862.3:c.3376C>A	NP_001005862.1:p.Pro1126Thr
NM_001289936.2:c.3421C>A	NP_001276865.1:p.Pro1141Thr
NM_001289937.2:c.*45C>A	NP_001276866.1:n.*45C>A
NM_001382782.1:c.3376C>A	NP_001369711.1:p.Pro1126Thr
NM_001382783.1:c.3376C>A	NP_001369712.1:p.Pro1126Thr
NM_001382784.1:c.3583C>A	NP_001369713.1:p.Pro1195Thr
NM_001382785.1:c.3568C>A	NP_001369714.1:p.Pro1190Thr
NM_001382786.1:c.3547C>A	NP_001369715.1:p.Pro1183Thr
NM_001382787.1:c.3541C>A	NP_001369716.1:p.Pro1181Thr
NM_001382788.1:c.3496C>A	NP_001369717.1:p.Pro1166Thr
NM_001382789.1:c.3487C>A	NP_001369718.1:p.Pro1163Thr
NM_001382790.1:c.3463C>A	NP_001369719.1:p.Pro1155Thr
NM_001382791.1:c.3457C>A	NP_001369720.1:p.Pro1153Thr
NM_001382792.1:c.3430C>A	NP_001369721.1:p.Pro1144Thr
NM_001382793.1:c.3424C>A	NP_001369722.1:p.Pro1142Thr
NM_001382794.1:c.3424C>A	NP_001369723.1:p.Pro1142Thr
NM_001382795.1:c.3418C>A	NP_001369724.1:p.Pro1140Thr
NM_001382796.1:c.3379C>A	NP_001369725.1:p.Pro1127Thr
NM_001382797.1:c.3367C>A	NP_001369726.1:p.Pro1123Thr
NM_001382798.1:c.3310C>A	NP_001369727.1:p.Pro1104Thr
NM_001382799.1:c.3286C>A	NP_001369728.1:p.Pro1096Thr
NM_001382800.1:c.3280C>A	NP_001369729.1:p.Pro1094Thr
NM_001382801.1:c.3262C>A	NP_001369730.1:p.Pro1088Thr
NM_001382802.1:c.3208C>A	NP_001369731.1:p.Pro1070Thr
NM_001382803.1:c.*45C>A	NP_001369732.1:n.*45C>A
NM_001382804.1:c.2638C>A	NP_001369733.1:p.Pro880Thr
NM_001382805.1:c.2515C>A	NP_001369734.1:p.Pro839Thr
NM_001382806.1:c.2428C>A	NP_001369735.1:p.Pro810Thr
NM_004448.4:c.3466C>A MANE Select	NP_004439.2:p.Pro1156Thr
NR_110535.2:n.3704C>A