Canonical Allele Identifier: CA499890872

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37884201C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727948C>T , CM000679.2:g.39727948C>T	GRCh38
NC_000017.10:g.37884201C>T , CM000679.1:g.37884201C>T	GRCh37
NC_000017.9:g.35137727C>T	NCBI36
NG_007503.1:g.44809C>T , LRG_724:g.44809C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3672C>T MANE Select	ENSP00000269571.4:p.Asp1224=
ENST00000269571.9:c.3672C>T	ENSP00000269571.4:p.Asp1224=
ENST00000406381.6:c.3582C>T	ENSP00000385185.2:p.Asp1194=
ENST00000445658.6:c.2844C>T	ENSP00000404047.2:p.Asp948=
ENST00000541774.5:c.3627C>T	ENSP00000446466.1:p.Asp1209=
ENST00000578373.5:c.*3462C>T	ENSP00000463427.1:n.*3462C>T
ENST00000584450.5:c.*251C>T	ENSP00000463714.1:n.*251C>T
ENST00000584601.5:c.3582C>T	ENSP00000462438.1:p.Asp1194=
NM_001005862.2:c.3582C>T , LRG_724t1:c.3582C>T	NP_001005862.1:p.Asp1194=
NM_001289936.1:c.3627C>T , LRG_724t4:c.3627C>T	NP_001276865.1:p.Asp1209=
NM_001289937.1:c.*251C>T	NP_001276866.1:n.*251C>T
NM_004448.3:c.3672C>T , LRG_724t2:c.3672C>T	NP_004439.2:p.Asp1224=
NR_110535.1:n.3996C>T
XM_024450641.1:c.3810C>T	XP_024306409.1:p.Asp1270=
XM_024450642.1:c.3765C>T	XP_024306410.1:p.Asp1255=
XM_024450643.1:c.3720C>T	XP_024306411.1:p.Asp1240=
NM_001005862.3:c.3582C>T	NP_001005862.1:p.Asp1194=
NM_001289936.2:c.3627C>T	NP_001276865.1:p.Asp1209=
NM_001289937.2:c.*251C>T	NP_001276866.1:n.*251C>T
NM_001382782.1:c.3582C>T	NP_001369711.1:p.Asp1194=
NM_001382783.1:c.3582C>T	NP_001369712.1:p.Asp1194=
NM_001382784.1:c.3789C>T	NP_001369713.1:p.Asp1263=
NM_001382785.1:c.3774C>T	NP_001369714.1:p.Asp1258=
NM_001382786.1:c.3753C>T	NP_001369715.1:p.Asp1251=
NM_001382787.1:c.3747C>T	NP_001369716.1:p.Asp1249=
NM_001382788.1:c.3702C>T	NP_001369717.1:p.Asp1234=
NM_001382789.1:c.3693C>T	NP_001369718.1:p.Asp1231=
NM_001382790.1:c.3669C>T	NP_001369719.1:p.Asp1223=
NM_001382791.1:c.3663C>T	NP_001369720.1:p.Asp1221=
NM_001382792.1:c.3636C>T	NP_001369721.1:p.Asp1212=
NM_001382793.1:c.3630C>T	NP_001369722.1:p.Asp1210=
NM_001382794.1:c.3630C>T	NP_001369723.1:p.Asp1210=
NM_001382795.1:c.3624C>T	NP_001369724.1:p.Asp1208=
NM_001382796.1:c.3585C>T	NP_001369725.1:p.Asp1195=
NM_001382797.1:c.3573C>T	NP_001369726.1:p.Asp1191=
NM_001382798.1:c.3516C>T	NP_001369727.1:p.Asp1172=
NM_001382799.1:c.3492C>T	NP_001369728.1:p.Asp1164=
NM_001382800.1:c.3486C>T	NP_001369729.1:p.Asp1162=
NM_001382801.1:c.3468C>T	NP_001369730.1:p.Asp1156=
NM_001382802.1:c.3414C>T	NP_001369731.1:p.Asp1138=
NM_001382803.1:c.*251C>T	NP_001369732.1:n.*251C>T
NM_001382804.1:c.2844C>T	NP_001369733.1:p.Asp948=
NM_001382805.1:c.2721C>T	NP_001369734.1:p.Asp907=
NM_001382806.1:c.2634C>T	NP_001369735.1:p.Asp878=
NM_004448.4:c.3672C>T MANE Select	NP_004439.2:p.Asp1224=
NR_110535.2:n.3910C>T