Canonical Allele Identifier: CA499890777

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37884123A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727870A>G , CM000679.2:g.39727870A>G	GRCh38
NC_000017.10:g.37884123A>G , CM000679.1:g.37884123A>G	GRCh37
NC_000017.9:g.35137649A>G	NCBI36
NG_007503.1:g.44731A>G , LRG_724:g.44731A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3594A>G MANE Select	ENSP00000269571.4:p.Thr1198=
ENST00000269571.9:c.3594A>G	ENSP00000269571.4:p.Thr1198=
ENST00000406381.6:c.3504A>G	ENSP00000385185.2:p.Thr1168=
ENST00000445658.6:c.2766A>G	ENSP00000404047.2:p.Thr922=
ENST00000541774.5:c.3549A>G	ENSP00000446466.1:p.Thr1183=
ENST00000578373.5:c.*3384A>G	ENSP00000463427.1:n.*3384A>G
ENST00000584450.5:c.*173A>G	ENSP00000463714.1:n.*173A>G
ENST00000584601.5:c.3504A>G	ENSP00000462438.1:p.Thr1168=
NM_001005862.2:c.3504A>G , LRG_724t1:c.3504A>G	NP_001005862.1:p.Thr1168=
NM_001289936.1:c.3549A>G , LRG_724t4:c.3549A>G	NP_001276865.1:p.Thr1183=
NM_001289937.1:c.*173A>G	NP_001276866.1:n.*173A>G
NM_004448.3:c.3594A>G , LRG_724t2:c.3594A>G	NP_004439.2:p.Thr1198=
NR_110535.1:n.3918A>G
XM_024450641.1:c.3732A>G	XP_024306409.1:p.Thr1244=
XM_024450642.1:c.3687A>G	XP_024306410.1:p.Thr1229=
XM_024450643.1:c.3642A>G	XP_024306411.1:p.Thr1214=
NM_001005862.3:c.3504A>G	NP_001005862.1:p.Thr1168=
NM_001289936.2:c.3549A>G	NP_001276865.1:p.Thr1183=
NM_001289937.2:c.*173A>G	NP_001276866.1:n.*173A>G
NM_001382782.1:c.3504A>G	NP_001369711.1:p.Thr1168=
NM_001382783.1:c.3504A>G	NP_001369712.1:p.Thr1168=
NM_001382784.1:c.3711A>G	NP_001369713.1:p.Thr1237=
NM_001382785.1:c.3696A>G	NP_001369714.1:p.Thr1232=
NM_001382786.1:c.3675A>G	NP_001369715.1:p.Thr1225=
NM_001382787.1:c.3669A>G	NP_001369716.1:p.Thr1223=
NM_001382788.1:c.3624A>G	NP_001369717.1:p.Thr1208=
NM_001382789.1:c.3615A>G	NP_001369718.1:p.Thr1205=
NM_001382790.1:c.3591A>G	NP_001369719.1:p.Thr1197=
NM_001382791.1:c.3585A>G	NP_001369720.1:p.Thr1195=
NM_001382792.1:c.3558A>G	NP_001369721.1:p.Thr1186=
NM_001382793.1:c.3552A>G	NP_001369722.1:p.Thr1184=
NM_001382794.1:c.3552A>G	NP_001369723.1:p.Thr1184=
NM_001382795.1:c.3546A>G	NP_001369724.1:p.Thr1182=
NM_001382796.1:c.3507A>G	NP_001369725.1:p.Thr1169=
NM_001382797.1:c.3495A>G	NP_001369726.1:p.Thr1165=
NM_001382798.1:c.3438A>G	NP_001369727.1:p.Thr1146=
NM_001382799.1:c.3414A>G	NP_001369728.1:p.Thr1138=
NM_001382800.1:c.3408A>G	NP_001369729.1:p.Thr1136=
NM_001382801.1:c.3390A>G	NP_001369730.1:p.Thr1130=
NM_001382802.1:c.3336A>G	NP_001369731.1:p.Thr1112=
NM_001382803.1:c.*173A>G	NP_001369732.1:n.*173A>G
NM_001382804.1:c.2766A>G	NP_001369733.1:p.Thr922=
NM_001382805.1:c.2643A>G	NP_001369734.1:p.Thr881=
NM_001382806.1:c.2556A>G	NP_001369735.1:p.Thr852=
NM_004448.4:c.3594A>G MANE Select	NP_004439.2:p.Thr1198=
NR_110535.2:n.3832A>G