Canonical Allele Identifier: CA399314495

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143314269
• MyVariant Identifiers: chr17:g.37884207C>G (hg19) ; chr17:g.39727954C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727954C>G , CM000679.2:g.39727954C>G	GRCh38
NC_000017.10:g.37884207C>G , CM000679.1:g.37884207C>G	GRCh37
NC_000017.9:g.35137733C>G	NCBI36
NG_007503.1:g.44815C>G , LRG_724:g.44815C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3678C>G MANE Select	ENSP00000269571.4:p.Asp1226Glu
ENST00000269571.9:c.3678C>G	ENSP00000269571.4:p.Asp1226Glu
ENST00000406381.6:c.3588C>G	ENSP00000385185.2:p.Asp1196Glu
ENST00000445658.6:c.2850C>G	ENSP00000404047.2:p.Asp950Glu
ENST00000541774.5:c.3633C>G	ENSP00000446466.1:p.Asp1211Glu
ENST00000578373.5:c.*3468C>G	ENSP00000463427.1:n.*3468C>G
ENST00000584450.5:c.*257C>G	ENSP00000463714.1:n.*257C>G
ENST00000584601.5:c.3588C>G	ENSP00000462438.1:p.Asp1196Glu
NM_001005862.2:c.3588C>G , LRG_724t1:c.3588C>G	NP_001005862.1:p.Asp1196Glu
NM_001289936.1:c.3633C>G , LRG_724t4:c.3633C>G	NP_001276865.1:p.Asp1211Glu
NM_001289937.1:c.*257C>G	NP_001276866.1:n.*257C>G
NM_004448.3:c.3678C>G , LRG_724t2:c.3678C>G	NP_004439.2:p.Asp1226Glu
NR_110535.1:n.4002C>G
XM_024450641.1:c.3816C>G	XP_024306409.1:p.Asp1272Glu
XM_024450642.1:c.3771C>G	XP_024306410.1:p.Asp1257Glu
XM_024450643.1:c.3726C>G	XP_024306411.1:p.Asp1242Glu
NM_001005862.3:c.3588C>G	NP_001005862.1:p.Asp1196Glu
NM_001289936.2:c.3633C>G	NP_001276865.1:p.Asp1211Glu
NM_001289937.2:c.*257C>G	NP_001276866.1:n.*257C>G
NM_001382782.1:c.3588C>G	NP_001369711.1:p.Asp1196Glu
NM_001382783.1:c.3588C>G	NP_001369712.1:p.Asp1196Glu
NM_001382784.1:c.3795C>G	NP_001369713.1:p.Asp1265Glu
NM_001382785.1:c.3780C>G	NP_001369714.1:p.Asp1260Glu
NM_001382786.1:c.3759C>G	NP_001369715.1:p.Asp1253Glu
NM_001382787.1:c.3753C>G	NP_001369716.1:p.Asp1251Glu
NM_001382788.1:c.3708C>G	NP_001369717.1:p.Asp1236Glu
NM_001382789.1:c.3699C>G	NP_001369718.1:p.Asp1233Glu
NM_001382790.1:c.3675C>G	NP_001369719.1:p.Asp1225Glu
NM_001382791.1:c.3669C>G	NP_001369720.1:p.Asp1223Glu
NM_001382792.1:c.3642C>G	NP_001369721.1:p.Asp1214Glu
NM_001382793.1:c.3636C>G	NP_001369722.1:p.Asp1212Glu
NM_001382794.1:c.3636C>G	NP_001369723.1:p.Asp1212Glu
NM_001382795.1:c.3630C>G	NP_001369724.1:p.Asp1210Glu
NM_001382796.1:c.3591C>G	NP_001369725.1:p.Asp1197Glu
NM_001382797.1:c.3579C>G	NP_001369726.1:p.Asp1193Glu
NM_001382798.1:c.3522C>G	NP_001369727.1:p.Asp1174Glu
NM_001382799.1:c.3498C>G	NP_001369728.1:p.Asp1166Glu
NM_001382800.1:c.3492C>G	NP_001369729.1:p.Asp1164Glu
NM_001382801.1:c.3474C>G	NP_001369730.1:p.Asp1158Glu
NM_001382802.1:c.3420C>G	NP_001369731.1:p.Asp1140Glu
NM_001382803.1:c.*257C>G	NP_001369732.1:n.*257C>G
NM_001382804.1:c.2850C>G	NP_001369733.1:p.Asp950Glu
NM_001382805.1:c.2727C>G	NP_001369734.1:p.Asp909Glu
NM_001382806.1:c.2640C>G	NP_001369735.1:p.Asp880Glu
NM_004448.4:c.3678C>G MANE Select	NP_004439.2:p.Asp1226Glu
NR_110535.2:n.3916C>G