Canonical Allele Identifier: CA499890782

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143306227
• MyVariant Identifiers: chr17:g.37884126C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727873C>T , CM000679.2:g.39727873C>T	GRCh38
NC_000017.10:g.37884126C>T , CM000679.1:g.37884126C>T	GRCh37
NC_000017.9:g.35137652C>T	NCBI36
NG_007503.1:g.44734C>T , LRG_724:g.44734C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3597C>T MANE Select	ENSP00000269571.4:p.Pro1199=
ENST00000269571.9:c.3597C>T	ENSP00000269571.4:p.Pro1199=
ENST00000406381.6:c.3507C>T	ENSP00000385185.2:p.Pro1169=
ENST00000445658.6:c.2769C>T	ENSP00000404047.2:p.Pro923=
ENST00000541774.5:c.3552C>T	ENSP00000446466.1:p.Pro1184=
ENST00000578373.5:c.*3387C>T	ENSP00000463427.1:n.*3387C>T
ENST00000584450.5:c.*176C>T	ENSP00000463714.1:n.*176C>T
ENST00000584601.5:c.3507C>T	ENSP00000462438.1:p.Pro1169=
NM_001005862.2:c.3507C>T , LRG_724t1:c.3507C>T	NP_001005862.1:p.Pro1169=
NM_001289936.1:c.3552C>T , LRG_724t4:c.3552C>T	NP_001276865.1:p.Pro1184=
NM_001289937.1:c.*176C>T	NP_001276866.1:n.*176C>T
NM_004448.3:c.3597C>T , LRG_724t2:c.3597C>T	NP_004439.2:p.Pro1199=
NR_110535.1:n.3921C>T
XM_024450641.1:c.3735C>T	XP_024306409.1:p.Pro1245=
XM_024450642.1:c.3690C>T	XP_024306410.1:p.Pro1230=
XM_024450643.1:c.3645C>T	XP_024306411.1:p.Pro1215=
NM_001005862.3:c.3507C>T	NP_001005862.1:p.Pro1169=
NM_001289936.2:c.3552C>T	NP_001276865.1:p.Pro1184=
NM_001289937.2:c.*176C>T	NP_001276866.1:n.*176C>T
NM_001382782.1:c.3507C>T	NP_001369711.1:p.Pro1169=
NM_001382783.1:c.3507C>T	NP_001369712.1:p.Pro1169=
NM_001382784.1:c.3714C>T	NP_001369713.1:p.Pro1238=
NM_001382785.1:c.3699C>T	NP_001369714.1:p.Pro1233=
NM_001382786.1:c.3678C>T	NP_001369715.1:p.Pro1226=
NM_001382787.1:c.3672C>T	NP_001369716.1:p.Pro1224=
NM_001382788.1:c.3627C>T	NP_001369717.1:p.Pro1209=
NM_001382789.1:c.3618C>T	NP_001369718.1:p.Pro1206=
NM_001382790.1:c.3594C>T	NP_001369719.1:p.Pro1198=
NM_001382791.1:c.3588C>T	NP_001369720.1:p.Pro1196=
NM_001382792.1:c.3561C>T	NP_001369721.1:p.Pro1187=
NM_001382793.1:c.3555C>T	NP_001369722.1:p.Pro1185=
NM_001382794.1:c.3555C>T	NP_001369723.1:p.Pro1185=
NM_001382795.1:c.3549C>T	NP_001369724.1:p.Pro1183=
NM_001382796.1:c.3510C>T	NP_001369725.1:p.Pro1170=
NM_001382797.1:c.3498C>T	NP_001369726.1:p.Pro1166=
NM_001382798.1:c.3441C>T	NP_001369727.1:p.Pro1147=
NM_001382799.1:c.3417C>T	NP_001369728.1:p.Pro1139=
NM_001382800.1:c.3411C>T	NP_001369729.1:p.Pro1137=
NM_001382801.1:c.3393C>T	NP_001369730.1:p.Pro1131=
NM_001382802.1:c.3339C>T	NP_001369731.1:p.Pro1113=
NM_001382803.1:c.*176C>T	NP_001369732.1:n.*176C>T
NM_001382804.1:c.2769C>T	NP_001369733.1:p.Pro923=
NM_001382805.1:c.2646C>T	NP_001369734.1:p.Pro882=
NM_001382806.1:c.2559C>T	NP_001369735.1:p.Pro853=
NM_004448.4:c.3597C>T MANE Select	NP_004439.2:p.Pro1199=
NR_110535.2:n.3835C>T