Canonical Allele Identifier: CA399313228

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37884041A>C (hg19) ; chr17:g.39727788A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727788A>C , CM000679.2:g.39727788A>C	GRCh38
NC_000017.10:g.37884041A>C , CM000679.1:g.37884041A>C	GRCh37
NC_000017.9:g.35137567A>C	NCBI36
NG_007503.1:g.44649A>C , LRG_724:g.44649A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3512A>C MANE Select	ENSP00000269571.4:p.Lys1171Thr
ENST00000269571.9:c.3512A>C	ENSP00000269571.4:p.Lys1171Thr
ENST00000406381.6:c.3422A>C	ENSP00000385185.2:p.Lys1141Thr
ENST00000445658.6:c.2684A>C	ENSP00000404047.2:p.Lys895Thr
ENST00000541774.5:c.3467A>C	ENSP00000446466.1:p.Lys1156Thr
ENST00000578373.5:c.*3302A>C	ENSP00000463427.1:n.*3302A>C
ENST00000584450.5:c.*91A>C	ENSP00000463714.1:n.*91A>C
ENST00000584601.5:c.3422A>C	ENSP00000462438.1:p.Lys1141Thr
NM_001005862.2:c.3422A>C , LRG_724t1:c.3422A>C	NP_001005862.1:p.Lys1141Thr
NM_001289936.1:c.3467A>C , LRG_724t4:c.3467A>C	NP_001276865.1:p.Lys1156Thr
NM_001289937.1:c.*91A>C	NP_001276866.1:n.*91A>C
NM_004448.3:c.3512A>C , LRG_724t2:c.3512A>C	NP_004439.2:p.Lys1171Thr
NR_110535.1:n.3836A>C
XM_024450641.1:c.3650A>C	XP_024306409.1:p.Lys1217Thr
XM_024450642.1:c.3605A>C	XP_024306410.1:p.Lys1202Thr
XM_024450643.1:c.3560A>C	XP_024306411.1:p.Lys1187Thr
NM_001005862.3:c.3422A>C	NP_001005862.1:p.Lys1141Thr
NM_001289936.2:c.3467A>C	NP_001276865.1:p.Lys1156Thr
NM_001289937.2:c.*91A>C	NP_001276866.1:n.*91A>C
NM_001382782.1:c.3422A>C	NP_001369711.1:p.Lys1141Thr
NM_001382783.1:c.3422A>C	NP_001369712.1:p.Lys1141Thr
NM_001382784.1:c.3629A>C	NP_001369713.1:p.Lys1210Thr
NM_001382785.1:c.3614A>C	NP_001369714.1:p.Lys1205Thr
NM_001382786.1:c.3593A>C	NP_001369715.1:p.Lys1198Thr
NM_001382787.1:c.3587A>C	NP_001369716.1:p.Lys1196Thr
NM_001382788.1:c.3542A>C	NP_001369717.1:p.Lys1181Thr
NM_001382789.1:c.3533A>C	NP_001369718.1:p.Lys1178Thr
NM_001382790.1:c.3509A>C	NP_001369719.1:p.Lys1170Thr
NM_001382791.1:c.3503A>C	NP_001369720.1:p.Lys1168Thr
NM_001382792.1:c.3476A>C	NP_001369721.1:p.Lys1159Thr
NM_001382793.1:c.3470A>C	NP_001369722.1:p.Lys1157Thr
NM_001382794.1:c.3470A>C	NP_001369723.1:p.Lys1157Thr
NM_001382795.1:c.3464A>C	NP_001369724.1:p.Lys1155Thr
NM_001382796.1:c.3425A>C	NP_001369725.1:p.Lys1142Thr
NM_001382797.1:c.3413A>C	NP_001369726.1:p.Lys1138Thr
NM_001382798.1:c.3356A>C	NP_001369727.1:p.Lys1119Thr
NM_001382799.1:c.3332A>C	NP_001369728.1:p.Lys1111Thr
NM_001382800.1:c.3326A>C	NP_001369729.1:p.Lys1109Thr
NM_001382801.1:c.3308A>C	NP_001369730.1:p.Lys1103Thr
NM_001382802.1:c.3254A>C	NP_001369731.1:p.Lys1085Thr
NM_001382803.1:c.*91A>C	NP_001369732.1:n.*91A>C
NM_001382804.1:c.2684A>C	NP_001369733.1:p.Lys895Thr
NM_001382805.1:c.2561A>C	NP_001369734.1:p.Lys854Thr
NM_001382806.1:c.2474A>C	NP_001369735.1:p.Lys825Thr
NM_004448.4:c.3512A>C MANE Select	NP_004439.2:p.Lys1171Thr
NR_110535.2:n.3750A>C