Canonical Allele Identifier: CA399313838

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143305952
• MyVariant Identifiers: chr17:g.37884122C>A (hg19) ; chr17:g.39727869C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727869C>A , CM000679.2:g.39727869C>A	GRCh38
NC_000017.10:g.37884122C>A , CM000679.1:g.37884122C>A	GRCh37
NC_000017.9:g.35137648C>A	NCBI36
NG_007503.1:g.44730C>A , LRG_724:g.44730C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3593C>A MANE Select	ENSP00000269571.4:p.Thr1198Lys
ENST00000269571.9:c.3593C>A	ENSP00000269571.4:p.Thr1198Lys
ENST00000406381.6:c.3503C>A	ENSP00000385185.2:p.Thr1168Lys
ENST00000445658.6:c.2765C>A	ENSP00000404047.2:p.Thr922Lys
ENST00000541774.5:c.3548C>A	ENSP00000446466.1:p.Thr1183Lys
ENST00000578373.5:c.*3383C>A	ENSP00000463427.1:n.*3383C>A
ENST00000584450.5:c.*172C>A	ENSP00000463714.1:n.*172C>A
ENST00000584601.5:c.3503C>A	ENSP00000462438.1:p.Thr1168Lys
NM_001005862.2:c.3503C>A , LRG_724t1:c.3503C>A	NP_001005862.1:p.Thr1168Lys
NM_001289936.1:c.3548C>A , LRG_724t4:c.3548C>A	NP_001276865.1:p.Thr1183Lys
NM_001289937.1:c.*172C>A	NP_001276866.1:n.*172C>A
NM_004448.3:c.3593C>A , LRG_724t2:c.3593C>A	NP_004439.2:p.Thr1198Lys
NR_110535.1:n.3917C>A
XM_024450641.1:c.3731C>A	XP_024306409.1:p.Thr1244Lys
XM_024450642.1:c.3686C>A	XP_024306410.1:p.Thr1229Lys
XM_024450643.1:c.3641C>A	XP_024306411.1:p.Thr1214Lys
NM_001005862.3:c.3503C>A	NP_001005862.1:p.Thr1168Lys
NM_001289936.2:c.3548C>A	NP_001276865.1:p.Thr1183Lys
NM_001289937.2:c.*172C>A	NP_001276866.1:n.*172C>A
NM_001382782.1:c.3503C>A	NP_001369711.1:p.Thr1168Lys
NM_001382783.1:c.3503C>A	NP_001369712.1:p.Thr1168Lys
NM_001382784.1:c.3710C>A	NP_001369713.1:p.Thr1237Lys
NM_001382785.1:c.3695C>A	NP_001369714.1:p.Thr1232Lys
NM_001382786.1:c.3674C>A	NP_001369715.1:p.Thr1225Lys
NM_001382787.1:c.3668C>A	NP_001369716.1:p.Thr1223Lys
NM_001382788.1:c.3623C>A	NP_001369717.1:p.Thr1208Lys
NM_001382789.1:c.3614C>A	NP_001369718.1:p.Thr1205Lys
NM_001382790.1:c.3590C>A	NP_001369719.1:p.Thr1197Lys
NM_001382791.1:c.3584C>A	NP_001369720.1:p.Thr1195Lys
NM_001382792.1:c.3557C>A	NP_001369721.1:p.Thr1186Lys
NM_001382793.1:c.3551C>A	NP_001369722.1:p.Thr1184Lys
NM_001382794.1:c.3551C>A	NP_001369723.1:p.Thr1184Lys
NM_001382795.1:c.3545C>A	NP_001369724.1:p.Thr1182Lys
NM_001382796.1:c.3506C>A	NP_001369725.1:p.Thr1169Lys
NM_001382797.1:c.3494C>A	NP_001369726.1:p.Thr1165Lys
NM_001382798.1:c.3437C>A	NP_001369727.1:p.Thr1146Lys
NM_001382799.1:c.3413C>A	NP_001369728.1:p.Thr1138Lys
NM_001382800.1:c.3407C>A	NP_001369729.1:p.Thr1136Lys
NM_001382801.1:c.3389C>A	NP_001369730.1:p.Thr1130Lys
NM_001382802.1:c.3335C>A	NP_001369731.1:p.Thr1112Lys
NM_001382803.1:c.*172C>A	NP_001369732.1:n.*172C>A
NM_001382804.1:c.2765C>A	NP_001369733.1:p.Thr922Lys
NM_001382805.1:c.2642C>A	NP_001369734.1:p.Thr881Lys
NM_001382806.1:c.2555C>A	NP_001369735.1:p.Thr852Lys
NM_004448.4:c.3593C>A MANE Select	NP_004439.2:p.Thr1198Lys
NR_110535.2:n.3831C>A