Canonical Allele Identifier: CA399313969

Gene: ERBB2

Linked Data

• dbSNP Id: rs201353217
• MyVariant Identifiers: chr17:g.37884142C>A (hg19) ; chr17:g.39727889C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727889C>A , CM000679.2:g.39727889C>A	GRCh38
NC_000017.10:g.37884142C>A , CM000679.1:g.37884142C>A	GRCh37
NC_000017.9:g.35137668C>A	NCBI36
NG_007503.1:g.44750C>A , LRG_724:g.44750C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3613C>A MANE Select	ENSP00000269571.4:p.Pro1205Thr
ENST00000269571.9:c.3613C>A	ENSP00000269571.4:p.Pro1205Thr
ENST00000406381.6:c.3523C>A	ENSP00000385185.2:p.Pro1175Thr
ENST00000445658.6:c.2785C>A	ENSP00000404047.2:p.Pro929Thr
ENST00000541774.5:c.3568C>A	ENSP00000446466.1:p.Pro1190Thr
ENST00000578373.5:c.*3403C>A	ENSP00000463427.1:n.*3403C>A
ENST00000584450.5:c.*192C>A	ENSP00000463714.1:n.*192C>A
ENST00000584601.5:c.3523C>A	ENSP00000462438.1:p.Pro1175Thr
NM_001005862.2:c.3523C>A , LRG_724t1:c.3523C>A	NP_001005862.1:p.Pro1175Thr
NM_001289936.1:c.3568C>A , LRG_724t4:c.3568C>A	NP_001276865.1:p.Pro1190Thr
NM_001289937.1:c.*192C>A	NP_001276866.1:n.*192C>A
NM_004448.3:c.3613C>A , LRG_724t2:c.3613C>A	NP_004439.2:p.Pro1205Thr
NR_110535.1:n.3937C>A
XM_024450641.1:c.3751C>A	XP_024306409.1:p.Pro1251Thr
XM_024450642.1:c.3706C>A	XP_024306410.1:p.Pro1236Thr
XM_024450643.1:c.3661C>A	XP_024306411.1:p.Pro1221Thr
NM_001005862.3:c.3523C>A	NP_001005862.1:p.Pro1175Thr
NM_001289936.2:c.3568C>A	NP_001276865.1:p.Pro1190Thr
NM_001289937.2:c.*192C>A	NP_001276866.1:n.*192C>A
NM_001382782.1:c.3523C>A	NP_001369711.1:p.Pro1175Thr
NM_001382783.1:c.3523C>A	NP_001369712.1:p.Pro1175Thr
NM_001382784.1:c.3730C>A	NP_001369713.1:p.Pro1244Thr
NM_001382785.1:c.3715C>A	NP_001369714.1:p.Pro1239Thr
NM_001382786.1:c.3694C>A	NP_001369715.1:p.Pro1232Thr
NM_001382787.1:c.3688C>A	NP_001369716.1:p.Pro1230Thr
NM_001382788.1:c.3643C>A	NP_001369717.1:p.Pro1215Thr
NM_001382789.1:c.3634C>A	NP_001369718.1:p.Pro1212Thr
NM_001382790.1:c.3610C>A	NP_001369719.1:p.Pro1204Thr
NM_001382791.1:c.3604C>A	NP_001369720.1:p.Pro1202Thr
NM_001382792.1:c.3577C>A	NP_001369721.1:p.Pro1193Thr
NM_001382793.1:c.3571C>A	NP_001369722.1:p.Pro1191Thr
NM_001382794.1:c.3571C>A	NP_001369723.1:p.Pro1191Thr
NM_001382795.1:c.3565C>A	NP_001369724.1:p.Pro1189Thr
NM_001382796.1:c.3526C>A	NP_001369725.1:p.Pro1176Thr
NM_001382797.1:c.3514C>A	NP_001369726.1:p.Pro1172Thr
NM_001382798.1:c.3457C>A	NP_001369727.1:p.Pro1153Thr
NM_001382799.1:c.3433C>A	NP_001369728.1:p.Pro1145Thr
NM_001382800.1:c.3427C>A	NP_001369729.1:p.Pro1143Thr
NM_001382801.1:c.3409C>A	NP_001369730.1:p.Pro1137Thr
NM_001382802.1:c.3355C>A	NP_001369731.1:p.Pro1119Thr
NM_001382803.1:c.*192C>A	NP_001369732.1:n.*192C>A
NM_001382804.1:c.2785C>A	NP_001369733.1:p.Pro929Thr
NM_001382805.1:c.2662C>A	NP_001369734.1:p.Pro888Thr
NM_001382806.1:c.2575C>A	NP_001369735.1:p.Pro859Thr
NM_004448.4:c.3613C>A MANE Select	NP_004439.2:p.Pro1205Thr
NR_110535.2:n.3851C>A