Canonical Allele Identifier: CA399312859

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143288175
• MyVariant Identifiers: chr17:g.37883960A>T (hg19) ; chr17:g.39727707A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727707A>T , CM000679.2:g.39727707A>T	GRCh38
NC_000017.10:g.37883960A>T , CM000679.1:g.37883960A>T	GRCh37
NC_000017.9:g.35137486A>T	NCBI36
NG_007503.1:g.44568A>T , LRG_724:g.44568A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3431A>T MANE Select	ENSP00000269571.4:p.Asp1144Val
ENST00000269571.9:c.3431A>T	ENSP00000269571.4:p.Asp1144Val
ENST00000406381.6:c.3341A>T	ENSP00000385185.2:p.Asp1114Val
ENST00000445658.6:c.2603A>T	ENSP00000404047.2:p.Asp868Val
ENST00000541774.5:c.3386A>T	ENSP00000446466.1:p.Asp1129Val
ENST00000578373.5:c.*3221A>T	ENSP00000463427.1:n.*3221A>T
ENST00000584450.5:c.*10A>T	ENSP00000463714.1:n.*10A>T
ENST00000584601.5:c.3341A>T	ENSP00000462438.1:p.Asp1114Val
NM_001005862.2:c.3341A>T , LRG_724t1:c.3341A>T	NP_001005862.1:p.Asp1114Val
NM_001289936.1:c.3386A>T , LRG_724t4:c.3386A>T	NP_001276865.1:p.Asp1129Val
NM_001289937.1:c.*10A>T	NP_001276866.1:n.*10A>T
NM_004448.3:c.3431A>T , LRG_724t2:c.3431A>T	NP_004439.2:p.Asp1144Val
NR_110535.1:n.3755A>T
XM_024450641.1:c.3569A>T	XP_024306409.1:p.Asp1190Val
XM_024450642.1:c.3524A>T	XP_024306410.1:p.Asp1175Val
XM_024450643.1:c.3479A>T	XP_024306411.1:p.Asp1160Val
NM_001005862.3:c.3341A>T	NP_001005862.1:p.Asp1114Val
NM_001289936.2:c.3386A>T	NP_001276865.1:p.Asp1129Val
NM_001289937.2:c.*10A>T	NP_001276866.1:n.*10A>T
NM_001382782.1:c.3341A>T	NP_001369711.1:p.Asp1114Val
NM_001382783.1:c.3341A>T	NP_001369712.1:p.Asp1114Val
NM_001382784.1:c.3548A>T	NP_001369713.1:p.Asp1183Val
NM_001382785.1:c.3533A>T	NP_001369714.1:p.Asp1178Val
NM_001382786.1:c.3512A>T	NP_001369715.1:p.Asp1171Val
NM_001382787.1:c.3506A>T	NP_001369716.1:p.Asp1169Val
NM_001382788.1:c.3461A>T	NP_001369717.1:p.Asp1154Val
NM_001382789.1:c.3452A>T	NP_001369718.1:p.Asp1151Val
NM_001382790.1:c.3428A>T	NP_001369719.1:p.Asp1143Val
NM_001382791.1:c.3422A>T	NP_001369720.1:p.Asp1141Val
NM_001382792.1:c.3395A>T	NP_001369721.1:p.Asp1132Val
NM_001382793.1:c.3389A>T	NP_001369722.1:p.Asp1130Val
NM_001382794.1:c.3389A>T	NP_001369723.1:p.Asp1130Val
NM_001382795.1:c.3383A>T	NP_001369724.1:p.Asp1128Val
NM_001382796.1:c.3344A>T	NP_001369725.1:p.Asp1115Val
NM_001382797.1:c.3332A>T	NP_001369726.1:p.Asp1111Val
NM_001382798.1:c.3275A>T	NP_001369727.1:p.Asp1092Val
NM_001382799.1:c.3251A>T	NP_001369728.1:p.Asp1084Val
NM_001382800.1:c.3245A>T	NP_001369729.1:p.Asp1082Val
NM_001382801.1:c.3227A>T	NP_001369730.1:p.Asp1076Val
NM_001382802.1:c.3173A>T	NP_001369731.1:p.Asp1058Val
NM_001382803.1:c.*10A>T	NP_001369732.1:n.*10A>T
NM_001382804.1:c.2603A>T	NP_001369733.1:p.Asp868Val
NM_001382805.1:c.2480A>T	NP_001369734.1:p.Asp827Val
NM_001382806.1:c.2393A>T	NP_001369735.1:p.Asp798Val
NM_004448.4:c.3431A>T MANE Select	NP_004439.2:p.Asp1144Val
NR_110535.2:n.3669A>T