Canonical Allele Identifier: CA399313642

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37884097G>T (hg19) ; chr17:g.39727844G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727844G>T , CM000679.2:g.39727844G>T	GRCh38
NC_000017.10:g.37884097G>T , CM000679.1:g.37884097G>T	GRCh37
NC_000017.9:g.35137623G>T	NCBI36
NG_007503.1:g.44705G>T , LRG_724:g.44705G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3568G>T MANE Select	ENSP00000269571.4:p.Ala1190Ser
ENST00000269571.9:c.3568G>T	ENSP00000269571.4:p.Ala1190Ser
ENST00000406381.6:c.3478G>T	ENSP00000385185.2:p.Ala1160Ser
ENST00000445658.6:c.2740G>T	ENSP00000404047.2:p.Ala914Ser
ENST00000541774.5:c.3523G>T	ENSP00000446466.1:p.Ala1175Ser
ENST00000578373.5:c.*3358G>T	ENSP00000463427.1:n.*3358G>T
ENST00000584450.5:c.*147G>T	ENSP00000463714.1:n.*147G>T
ENST00000584601.5:c.3478G>T	ENSP00000462438.1:p.Ala1160Ser
NM_001005862.2:c.3478G>T , LRG_724t1:c.3478G>T	NP_001005862.1:p.Ala1160Ser
NM_001289936.1:c.3523G>T , LRG_724t4:c.3523G>T	NP_001276865.1:p.Ala1175Ser
NM_001289937.1:c.*147G>T	NP_001276866.1:n.*147G>T
NM_004448.3:c.3568G>T , LRG_724t2:c.3568G>T	NP_004439.2:p.Ala1190Ser
NR_110535.1:n.3892G>T
XM_024450641.1:c.3706G>T	XP_024306409.1:p.Ala1236Ser
XM_024450642.1:c.3661G>T	XP_024306410.1:p.Ala1221Ser
XM_024450643.1:c.3616G>T	XP_024306411.1:p.Ala1206Ser
NM_001005862.3:c.3478G>T	NP_001005862.1:p.Ala1160Ser
NM_001289936.2:c.3523G>T	NP_001276865.1:p.Ala1175Ser
NM_001289937.2:c.*147G>T	NP_001276866.1:n.*147G>T
NM_001382782.1:c.3478G>T	NP_001369711.1:p.Ala1160Ser
NM_001382783.1:c.3478G>T	NP_001369712.1:p.Ala1160Ser
NM_001382784.1:c.3685G>T	NP_001369713.1:p.Ala1229Ser
NM_001382785.1:c.3670G>T	NP_001369714.1:p.Ala1224Ser
NM_001382786.1:c.3649G>T	NP_001369715.1:p.Ala1217Ser
NM_001382787.1:c.3643G>T	NP_001369716.1:p.Ala1215Ser
NM_001382788.1:c.3598G>T	NP_001369717.1:p.Ala1200Ser
NM_001382789.1:c.3589G>T	NP_001369718.1:p.Ala1197Ser
NM_001382790.1:c.3565G>T	NP_001369719.1:p.Ala1189Ser
NM_001382791.1:c.3559G>T	NP_001369720.1:p.Ala1187Ser
NM_001382792.1:c.3532G>T	NP_001369721.1:p.Ala1178Ser
NM_001382793.1:c.3526G>T	NP_001369722.1:p.Ala1176Ser
NM_001382794.1:c.3526G>T	NP_001369723.1:p.Ala1176Ser
NM_001382795.1:c.3520G>T	NP_001369724.1:p.Ala1174Ser
NM_001382796.1:c.3481G>T	NP_001369725.1:p.Ala1161Ser
NM_001382797.1:c.3469G>T	NP_001369726.1:p.Ala1157Ser
NM_001382798.1:c.3412G>T	NP_001369727.1:p.Ala1138Ser
NM_001382799.1:c.3388G>T	NP_001369728.1:p.Ala1130Ser
NM_001382800.1:c.3382G>T	NP_001369729.1:p.Ala1128Ser
NM_001382801.1:c.3364G>T	NP_001369730.1:p.Ala1122Ser
NM_001382802.1:c.3310G>T	NP_001369731.1:p.Ala1104Ser
NM_001382803.1:c.*147G>T	NP_001369732.1:n.*147G>T
NM_001382804.1:c.2740G>T	NP_001369733.1:p.Ala914Ser
NM_001382805.1:c.2617G>T	NP_001369734.1:p.Ala873Ser
NM_001382806.1:c.2530G>T	NP_001369735.1:p.Ala844Ser
NM_004448.4:c.3568G>T MANE Select	NP_004439.2:p.Ala1190Ser
NR_110535.2:n.3806G>T