Canonical Allele Identifier: CA399313286

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37884049T>G (hg19) ; chr17:g.39727796T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727796T>G , CM000679.2:g.39727796T>G	GRCh38
NC_000017.10:g.37884049T>G , CM000679.1:g.37884049T>G	GRCh37
NC_000017.9:g.35137575T>G	NCBI36
NG_007503.1:g.44657T>G , LRG_724:g.44657T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3520T>G MANE Select	ENSP00000269571.4:p.Ser1174Ala
ENST00000269571.9:c.3520T>G	ENSP00000269571.4:p.Ser1174Ala
ENST00000406381.6:c.3430T>G	ENSP00000385185.2:p.Ser1144Ala
ENST00000445658.6:c.2692T>G	ENSP00000404047.2:p.Ser898Ala
ENST00000541774.5:c.3475T>G	ENSP00000446466.1:p.Ser1159Ala
ENST00000578373.5:c.*3310T>G	ENSP00000463427.1:n.*3310T>G
ENST00000584450.5:c.*99T>G	ENSP00000463714.1:n.*99T>G
ENST00000584601.5:c.3430T>G	ENSP00000462438.1:p.Ser1144Ala
NM_001005862.2:c.3430T>G , LRG_724t1:c.3430T>G	NP_001005862.1:p.Ser1144Ala
NM_001289936.1:c.3475T>G , LRG_724t4:c.3475T>G	NP_001276865.1:p.Ser1159Ala
NM_001289937.1:c.*99T>G	NP_001276866.1:n.*99T>G
NM_004448.3:c.3520T>G , LRG_724t2:c.3520T>G	NP_004439.2:p.Ser1174Ala
NR_110535.1:n.3844T>G
XM_024450641.1:c.3658T>G	XP_024306409.1:p.Ser1220Ala
XM_024450642.1:c.3613T>G	XP_024306410.1:p.Ser1205Ala
XM_024450643.1:c.3568T>G	XP_024306411.1:p.Ser1190Ala
NM_001005862.3:c.3430T>G	NP_001005862.1:p.Ser1144Ala
NM_001289936.2:c.3475T>G	NP_001276865.1:p.Ser1159Ala
NM_001289937.2:c.*99T>G	NP_001276866.1:n.*99T>G
NM_001382782.1:c.3430T>G	NP_001369711.1:p.Ser1144Ala
NM_001382783.1:c.3430T>G	NP_001369712.1:p.Ser1144Ala
NM_001382784.1:c.3637T>G	NP_001369713.1:p.Ser1213Ala
NM_001382785.1:c.3622T>G	NP_001369714.1:p.Ser1208Ala
NM_001382786.1:c.3601T>G	NP_001369715.1:p.Ser1201Ala
NM_001382787.1:c.3595T>G	NP_001369716.1:p.Ser1199Ala
NM_001382788.1:c.3550T>G	NP_001369717.1:p.Ser1184Ala
NM_001382789.1:c.3541T>G	NP_001369718.1:p.Ser1181Ala
NM_001382790.1:c.3517T>G	NP_001369719.1:p.Ser1173Ala
NM_001382791.1:c.3511T>G	NP_001369720.1:p.Ser1171Ala
NM_001382792.1:c.3484T>G	NP_001369721.1:p.Ser1162Ala
NM_001382793.1:c.3478T>G	NP_001369722.1:p.Ser1160Ala
NM_001382794.1:c.3478T>G	NP_001369723.1:p.Ser1160Ala
NM_001382795.1:c.3472T>G	NP_001369724.1:p.Ser1158Ala
NM_001382796.1:c.3433T>G	NP_001369725.1:p.Ser1145Ala
NM_001382797.1:c.3421T>G	NP_001369726.1:p.Ser1141Ala
NM_001382798.1:c.3364T>G	NP_001369727.1:p.Ser1122Ala
NM_001382799.1:c.3340T>G	NP_001369728.1:p.Ser1114Ala
NM_001382800.1:c.3334T>G	NP_001369729.1:p.Ser1112Ala
NM_001382801.1:c.3316T>G	NP_001369730.1:p.Ser1106Ala
NM_001382802.1:c.3262T>G	NP_001369731.1:p.Ser1088Ala
NM_001382803.1:c.*99T>G	NP_001369732.1:n.*99T>G
NM_001382804.1:c.2692T>G	NP_001369733.1:p.Ser898Ala
NM_001382805.1:c.2569T>G	NP_001369734.1:p.Ser857Ala
NM_001382806.1:c.2482T>G	NP_001369735.1:p.Ser828Ala
NM_004448.4:c.3520T>G MANE Select	NP_004439.2:p.Ser1174Ala
NR_110535.2:n.3758T>G