Canonical Allele Identifier: CA499890890

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143314752
• MyVariant Identifiers: chr17:g.37884213A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727960A>G , CM000679.2:g.39727960A>G	GRCh38
NC_000017.10:g.37884213A>G , CM000679.1:g.37884213A>G	GRCh37
NC_000017.9:g.35137739A>G	NCBI36
NG_007503.1:g.44821A>G , LRG_724:g.44821A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3684A>G MANE Select	ENSP00000269571.4:p.Pro1228=
ENST00000269571.9:c.3684A>G	ENSP00000269571.4:p.Pro1228=
ENST00000406381.6:c.3594A>G	ENSP00000385185.2:p.Pro1198=
ENST00000445658.6:c.2856A>G	ENSP00000404047.2:p.Pro952=
ENST00000541774.5:c.3639A>G	ENSP00000446466.1:p.Pro1213=
ENST00000578373.5:c.*3474A>G	ENSP00000463427.1:n.*3474A>G
ENST00000584450.5:c.*263A>G	ENSP00000463714.1:n.*263A>G
ENST00000584601.5:c.3594A>G	ENSP00000462438.1:p.Pro1198=
NM_001005862.2:c.3594A>G , LRG_724t1:c.3594A>G	NP_001005862.1:p.Pro1198=
NM_001289936.1:c.3639A>G , LRG_724t4:c.3639A>G	NP_001276865.1:p.Pro1213=
NM_001289937.1:c.*263A>G	NP_001276866.1:n.*263A>G
NM_004448.3:c.3684A>G , LRG_724t2:c.3684A>G	NP_004439.2:p.Pro1228=
NR_110535.1:n.4008A>G
XM_024450641.1:c.3822A>G	XP_024306409.1:p.Pro1274=
XM_024450642.1:c.3777A>G	XP_024306410.1:p.Pro1259=
XM_024450643.1:c.3732A>G	XP_024306411.1:p.Pro1244=
NM_001005862.3:c.3594A>G	NP_001005862.1:p.Pro1198=
NM_001289936.2:c.3639A>G	NP_001276865.1:p.Pro1213=
NM_001289937.2:c.*263A>G	NP_001276866.1:n.*263A>G
NM_001382782.1:c.3594A>G	NP_001369711.1:p.Pro1198=
NM_001382783.1:c.3594A>G	NP_001369712.1:p.Pro1198=
NM_001382784.1:c.3801A>G	NP_001369713.1:p.Pro1267=
NM_001382785.1:c.3786A>G	NP_001369714.1:p.Pro1262=
NM_001382786.1:c.3765A>G	NP_001369715.1:p.Pro1255=
NM_001382787.1:c.3759A>G	NP_001369716.1:p.Pro1253=
NM_001382788.1:c.3714A>G	NP_001369717.1:p.Pro1238=
NM_001382789.1:c.3705A>G	NP_001369718.1:p.Pro1235=
NM_001382790.1:c.3681A>G	NP_001369719.1:p.Pro1227=
NM_001382791.1:c.3675A>G	NP_001369720.1:p.Pro1225=
NM_001382792.1:c.3648A>G	NP_001369721.1:p.Pro1216=
NM_001382793.1:c.3642A>G	NP_001369722.1:p.Pro1214=
NM_001382794.1:c.3642A>G	NP_001369723.1:p.Pro1214=
NM_001382795.1:c.3636A>G	NP_001369724.1:p.Pro1212=
NM_001382796.1:c.3597A>G	NP_001369725.1:p.Pro1199=
NM_001382797.1:c.3585A>G	NP_001369726.1:p.Pro1195=
NM_001382798.1:c.3528A>G	NP_001369727.1:p.Pro1176=
NM_001382799.1:c.3504A>G	NP_001369728.1:p.Pro1168=
NM_001382800.1:c.3498A>G	NP_001369729.1:p.Pro1166=
NM_001382801.1:c.3480A>G	NP_001369730.1:p.Pro1160=
NM_001382802.1:c.3426A>G	NP_001369731.1:p.Pro1142=
NM_001382803.1:c.*263A>G	NP_001369732.1:n.*263A>G
NM_001382804.1:c.2856A>G	NP_001369733.1:p.Pro952=
NM_001382805.1:c.2733A>G	NP_001369734.1:p.Pro911=
NM_001382806.1:c.2646A>G	NP_001369735.1:p.Pro882=
NM_004448.4:c.3684A>G MANE Select	NP_004439.2:p.Pro1228=
NR_110535.2:n.3922A>G