Canonical Allele Identifier: CA399314429

Gene: ERBB2

Linked Data

• dbSNP Id: rs2059871595
• MyVariant Identifiers: chr17:g.37884199G>C (hg19) ; chr17:g.39727946G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727946G>C , CM000679.2:g.39727946G>C	GRCh38
NC_000017.10:g.37884199G>C , CM000679.1:g.37884199G>C	GRCh37
NC_000017.9:g.35137725G>C	NCBI36
NG_007503.1:g.44807G>C , LRG_724:g.44807G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3670G>C MANE Select	ENSP00000269571.4:p.Asp1224His
ENST00000269571.9:c.3670G>C	ENSP00000269571.4:p.Asp1224His
ENST00000406381.6:c.3580G>C	ENSP00000385185.2:p.Asp1194His
ENST00000445658.6:c.2842G>C	ENSP00000404047.2:p.Asp948His
ENST00000541774.5:c.3625G>C	ENSP00000446466.1:p.Asp1209His
ENST00000578373.5:c.*3460G>C	ENSP00000463427.1:n.*3460G>C
ENST00000584450.5:c.*249G>C	ENSP00000463714.1:n.*249G>C
ENST00000584601.5:c.3580G>C	ENSP00000462438.1:p.Asp1194His
NM_001005862.2:c.3580G>C , LRG_724t1:c.3580G>C	NP_001005862.1:p.Asp1194His
NM_001289936.1:c.3625G>C , LRG_724t4:c.3625G>C	NP_001276865.1:p.Asp1209His
NM_001289937.1:c.*249G>C	NP_001276866.1:n.*249G>C
NM_004448.3:c.3670G>C , LRG_724t2:c.3670G>C	NP_004439.2:p.Asp1224His
NR_110535.1:n.3994G>C
XM_024450641.1:c.3808G>C	XP_024306409.1:p.Asp1270His
XM_024450642.1:c.3763G>C	XP_024306410.1:p.Asp1255His
XM_024450643.1:c.3718G>C	XP_024306411.1:p.Asp1240His
NM_001005862.3:c.3580G>C	NP_001005862.1:p.Asp1194His
NM_001289936.2:c.3625G>C	NP_001276865.1:p.Asp1209His
NM_001289937.2:c.*249G>C	NP_001276866.1:n.*249G>C
NM_001382782.1:c.3580G>C	NP_001369711.1:p.Asp1194His
NM_001382783.1:c.3580G>C	NP_001369712.1:p.Asp1194His
NM_001382784.1:c.3787G>C	NP_001369713.1:p.Asp1263His
NM_001382785.1:c.3772G>C	NP_001369714.1:p.Asp1258His
NM_001382786.1:c.3751G>C	NP_001369715.1:p.Asp1251His
NM_001382787.1:c.3745G>C	NP_001369716.1:p.Asp1249His
NM_001382788.1:c.3700G>C	NP_001369717.1:p.Asp1234His
NM_001382789.1:c.3691G>C	NP_001369718.1:p.Asp1231His
NM_001382790.1:c.3667G>C	NP_001369719.1:p.Asp1223His
NM_001382791.1:c.3661G>C	NP_001369720.1:p.Asp1221His
NM_001382792.1:c.3634G>C	NP_001369721.1:p.Asp1212His
NM_001382793.1:c.3628G>C	NP_001369722.1:p.Asp1210His
NM_001382794.1:c.3628G>C	NP_001369723.1:p.Asp1210His
NM_001382795.1:c.3622G>C	NP_001369724.1:p.Asp1208His
NM_001382796.1:c.3583G>C	NP_001369725.1:p.Asp1195His
NM_001382797.1:c.3571G>C	NP_001369726.1:p.Asp1191His
NM_001382798.1:c.3514G>C	NP_001369727.1:p.Asp1172His
NM_001382799.1:c.3490G>C	NP_001369728.1:p.Asp1164His
NM_001382800.1:c.3484G>C	NP_001369729.1:p.Asp1162His
NM_001382801.1:c.3466G>C	NP_001369730.1:p.Asp1156His
NM_001382802.1:c.3412G>C	NP_001369731.1:p.Asp1138His
NM_001382803.1:c.*249G>C	NP_001369732.1:n.*249G>C
NM_001382804.1:c.2842G>C	NP_001369733.1:p.Asp948His
NM_001382805.1:c.2719G>C	NP_001369734.1:p.Asp907His
NM_001382806.1:c.2632G>C	NP_001369735.1:p.Asp878His
NM_004448.4:c.3670G>C MANE Select	NP_004439.2:p.Asp1224His
NR_110535.2:n.3908G>C