Canonical Allele Identifier: CA399314447

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37884201C>A (hg19) ; chr17:g.39727948C>A (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3672C>A MANE Select	ENSP00000269571.4:p.Asp1224Glu
ENST00000269571.9:c.3672C>A	ENSP00000269571.4:p.Asp1224Glu
ENST00000406381.6:c.3582C>A	ENSP00000385185.2:p.Asp1194Glu
ENST00000445658.6:c.2844C>A	ENSP00000404047.2:p.Asp948Glu
ENST00000541774.5:c.3627C>A	ENSP00000446466.1:p.Asp1209Glu
ENST00000578373.5:c.*3462C>A	ENSP00000463427.1:n.*3462C>A
ENST00000584450.5:c.*251C>A	ENSP00000463714.1:n.*251C>A
ENST00000584601.5:c.3582C>A	ENSP00000462438.1:p.Asp1194Glu
NM_001005862.2:c.3582C>A , LRG_724t1:c.3582C>A	NP_001005862.1:p.Asp1194Glu
NM_001289936.1:c.3627C>A , LRG_724t4:c.3627C>A	NP_001276865.1:p.Asp1209Glu
NM_001289937.1:c.*251C>A	NP_001276866.1:n.*251C>A
NM_004448.3:c.3672C>A , LRG_724t2:c.3672C>A	NP_004439.2:p.Asp1224Glu
NR_110535.1:n.3996C>A
XM_024450641.1:c.3810C>A	XP_024306409.1:p.Asp1270Glu
XM_024450642.1:c.3765C>A	XP_024306410.1:p.Asp1255Glu
XM_024450643.1:c.3720C>A	XP_024306411.1:p.Asp1240Glu
NM_001005862.3:c.3582C>A	NP_001005862.1:p.Asp1194Glu
NM_001289936.2:c.3627C>A	NP_001276865.1:p.Asp1209Glu
NM_001289937.2:c.*251C>A	NP_001276866.1:n.*251C>A
NM_001382782.1:c.3582C>A	NP_001369711.1:p.Asp1194Glu
NM_001382783.1:c.3582C>A	NP_001369712.1:p.Asp1194Glu
NM_001382784.1:c.3789C>A	NP_001369713.1:p.Asp1263Glu
NM_001382785.1:c.3774C>A	NP_001369714.1:p.Asp1258Glu
NM_001382786.1:c.3753C>A	NP_001369715.1:p.Asp1251Glu
NM_001382787.1:c.3747C>A	NP_001369716.1:p.Asp1249Glu
NM_001382788.1:c.3702C>A	NP_001369717.1:p.Asp1234Glu
NM_001382789.1:c.3693C>A	NP_001369718.1:p.Asp1231Glu
NM_001382790.1:c.3669C>A	NP_001369719.1:p.Asp1223Glu
NM_001382791.1:c.3663C>A	NP_001369720.1:p.Asp1221Glu
NM_001382792.1:c.3636C>A	NP_001369721.1:p.Asp1212Glu
NM_001382793.1:c.3630C>A	NP_001369722.1:p.Asp1210Glu
NM_001382794.1:c.3630C>A	NP_001369723.1:p.Asp1210Glu
NM_001382795.1:c.3624C>A	NP_001369724.1:p.Asp1208Glu
NM_001382796.1:c.3585C>A	NP_001369725.1:p.Asp1195Glu
NM_001382797.1:c.3573C>A	NP_001369726.1:p.Asp1191Glu
NM_001382798.1:c.3516C>A	NP_001369727.1:p.Asp1172Glu
NM_001382799.1:c.3492C>A	NP_001369728.1:p.Asp1164Glu
NM_001382800.1:c.3486C>A	NP_001369729.1:p.Asp1162Glu
NM_001382801.1:c.3468C>A	NP_001369730.1:p.Asp1156Glu
NM_001382802.1:c.3414C>A	NP_001369731.1:p.Asp1138Glu
NM_001382803.1:c.*251C>A	NP_001369732.1:n.*251C>A
NM_001382804.1:c.2844C>A	NP_001369733.1:p.Asp948Glu
NM_001382805.1:c.2721C>A	NP_001369734.1:p.Asp907Glu
NM_001382806.1:c.2634C>A	NP_001369735.1:p.Asp878Glu
NM_004448.4:c.3672C>A MANE Select	NP_004439.2:p.Asp1224Glu
NR_110535.2:n.3910C>A