Canonical Allele Identifier: CA399313068

Gene: ERBB2

Linked Data

• dbSNP Id: rs959969530
• MyVariant Identifiers: chr17:g.37884016G>T (hg19) ; chr17:g.39727763G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727763G>T , CM000679.2:g.39727763G>T	GRCh38
NC_000017.10:g.37884016G>T , CM000679.1:g.37884016G>T	GRCh37
NC_000017.9:g.35137542G>T	NCBI36
NG_007503.1:g.44624G>T , LRG_724:g.44624G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3487G>T MANE Select	ENSP00000269571.4:p.Ala1163Ser
ENST00000269571.9:c.3487G>T	ENSP00000269571.4:p.Ala1163Ser
ENST00000406381.6:c.3397G>T	ENSP00000385185.2:p.Ala1133Ser
ENST00000445658.6:c.2659G>T	ENSP00000404047.2:p.Ala887Ser
ENST00000541774.5:c.3442G>T	ENSP00000446466.1:p.Ala1148Ser
ENST00000578373.5:c.*3277G>T	ENSP00000463427.1:n.*3277G>T
ENST00000584450.5:c.*66G>T	ENSP00000463714.1:n.*66G>T
ENST00000584601.5:c.3397G>T	ENSP00000462438.1:p.Ala1133Ser
NM_001005862.2:c.3397G>T , LRG_724t1:c.3397G>T	NP_001005862.1:p.Ala1133Ser
NM_001289936.1:c.3442G>T , LRG_724t4:c.3442G>T	NP_001276865.1:p.Ala1148Ser
NM_001289937.1:c.*66G>T	NP_001276866.1:n.*66G>T
NM_004448.3:c.3487G>T , LRG_724t2:c.3487G>T	NP_004439.2:p.Ala1163Ser
NR_110535.1:n.3811G>T
XM_024450641.1:c.3625G>T	XP_024306409.1:p.Ala1209Ser
XM_024450642.1:c.3580G>T	XP_024306410.1:p.Ala1194Ser
XM_024450643.1:c.3535G>T	XP_024306411.1:p.Ala1179Ser
NM_001005862.3:c.3397G>T	NP_001005862.1:p.Ala1133Ser
NM_001289936.2:c.3442G>T	NP_001276865.1:p.Ala1148Ser
NM_001289937.2:c.*66G>T	NP_001276866.1:n.*66G>T
NM_001382782.1:c.3397G>T	NP_001369711.1:p.Ala1133Ser
NM_001382783.1:c.3397G>T	NP_001369712.1:p.Ala1133Ser
NM_001382784.1:c.3604G>T	NP_001369713.1:p.Ala1202Ser
NM_001382785.1:c.3589G>T	NP_001369714.1:p.Ala1197Ser
NM_001382786.1:c.3568G>T	NP_001369715.1:p.Ala1190Ser
NM_001382787.1:c.3562G>T	NP_001369716.1:p.Ala1188Ser
NM_001382788.1:c.3517G>T	NP_001369717.1:p.Ala1173Ser
NM_001382789.1:c.3508G>T	NP_001369718.1:p.Ala1170Ser
NM_001382790.1:c.3484G>T	NP_001369719.1:p.Ala1162Ser
NM_001382791.1:c.3478G>T	NP_001369720.1:p.Ala1160Ser
NM_001382792.1:c.3451G>T	NP_001369721.1:p.Ala1151Ser
NM_001382793.1:c.3445G>T	NP_001369722.1:p.Ala1149Ser
NM_001382794.1:c.3445G>T	NP_001369723.1:p.Ala1149Ser
NM_001382795.1:c.3439G>T	NP_001369724.1:p.Ala1147Ser
NM_001382796.1:c.3400G>T	NP_001369725.1:p.Ala1134Ser
NM_001382797.1:c.3388G>T	NP_001369726.1:p.Ala1130Ser
NM_001382798.1:c.3331G>T	NP_001369727.1:p.Ala1111Ser
NM_001382799.1:c.3307G>T	NP_001369728.1:p.Ala1103Ser
NM_001382800.1:c.3301G>T	NP_001369729.1:p.Ala1101Ser
NM_001382801.1:c.3283G>T	NP_001369730.1:p.Ala1095Ser
NM_001382802.1:c.3229G>T	NP_001369731.1:p.Ala1077Ser
NM_001382803.1:c.*66G>T	NP_001369732.1:n.*66G>T
NM_001382804.1:c.2659G>T	NP_001369733.1:p.Ala887Ser
NM_001382805.1:c.2536G>T	NP_001369734.1:p.Ala846Ser
NM_001382806.1:c.2449G>T	NP_001369735.1:p.Ala817Ser
NM_004448.4:c.3487G>T MANE Select	NP_004439.2:p.Ala1163Ser
NR_110535.2:n.3725G>T