Canonical Allele Identifier: CA399310878

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37883690T>G (hg19) ; chr17:g.39727437T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727437T>G , CM000679.2:g.39727437T>G	GRCh38
NC_000017.10:g.37883690T>G , CM000679.1:g.37883690T>G	GRCh37
NC_000017.9:g.35137216T>G	NCBI36
NG_007503.1:g.44298T>G , LRG_724:g.44298T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3302T>G MANE Select	ENSP00000269571.4:p.Leu1101Arg
ENST00000269571.9:c.3302T>G	ENSP00000269571.4:p.Leu1101Arg
ENST00000406381.6:c.3212T>G	ENSP00000385185.2:p.Leu1071Arg
ENST00000445658.6:c.2474T>G	ENSP00000404047.2:p.Leu825Arg
ENST00000541774.5:c.3257T>G	ENSP00000446466.1:p.Leu1086Arg
ENST00000578373.5:c.*3092T>G	ENSP00000463427.1:n.*3092T>G
ENST00000584450.5:c.3160-252T>G	ENSP00000463714.1:n.3160-252T>G
ENST00000584601.5:c.3212T>G	ENSP00000462438.1:p.Leu1071Arg
NM_001005862.2:c.3212T>G , LRG_724t1:c.3212T>G	NP_001005862.1:p.Leu1071Arg
NM_001289936.1:c.3257T>G , LRG_724t4:c.3257T>G	NP_001276865.1:p.Leu1086Arg
NM_001289937.1:c.3160-252T>G	NP_001276866.1:n.3160-252T>G
NM_004448.3:c.3302T>G , LRG_724t2:c.3302T>G	NP_004439.2:p.Leu1101Arg
NR_110535.1:n.3626T>G
XM_024450641.1:c.3440T>G	XP_024306409.1:p.Leu1147Arg
XM_024450642.1:c.3395T>G	XP_024306410.1:p.Leu1132Arg
XM_024450643.1:c.3350T>G	XP_024306411.1:p.Leu1117Arg
NM_001005862.3:c.3212T>G	NP_001005862.1:p.Leu1071Arg
NM_001289936.2:c.3257T>G	NP_001276865.1:p.Leu1086Arg
NM_001289937.2:c.3160-252T>G	NP_001276866.1:n.3160-252T>G
NM_001382782.1:c.3212T>G	NP_001369711.1:p.Leu1071Arg
NM_001382783.1:c.3212T>G	NP_001369712.1:p.Leu1071Arg
NM_001382784.1:c.3419T>G	NP_001369713.1:p.Leu1140Arg
NM_001382785.1:c.3404T>G	NP_001369714.1:p.Leu1135Arg
NM_001382786.1:c.3383T>G	NP_001369715.1:p.Leu1128Arg
NM_001382787.1:c.3377T>G	NP_001369716.1:p.Leu1126Arg
NM_001382788.1:c.3332T>G	NP_001369717.1:p.Leu1111Arg
NM_001382789.1:c.3323T>G	NP_001369718.1:p.Leu1108Arg
NM_001382790.1:c.3299T>G	NP_001369719.1:p.Leu1100Arg
NM_001382791.1:c.3293T>G	NP_001369720.1:p.Leu1098Arg
NM_001382792.1:c.3266T>G	NP_001369721.1:p.Leu1089Arg
NM_001382793.1:c.3260T>G	NP_001369722.1:p.Leu1087Arg
NM_001382794.1:c.3260T>G	NP_001369723.1:p.Leu1087Arg
NM_001382795.1:c.3254T>G	NP_001369724.1:p.Leu1085Arg
NM_001382796.1:c.3215T>G	NP_001369725.1:p.Leu1072Arg
NM_001382797.1:c.3203T>G	NP_001369726.1:p.Leu1068Arg
NM_001382798.1:c.3146T>G	NP_001369727.1:p.Leu1049Arg
NM_001382799.1:c.3122T>G	NP_001369728.1:p.Leu1041Arg
NM_001382800.1:c.3116T>G	NP_001369729.1:p.Leu1039Arg
NM_001382801.1:c.3098T>G	NP_001369730.1:p.Leu1033Arg
NM_001382802.1:c.3044T>G	NP_001369731.1:p.Leu1015Arg
NM_001382803.1:c.3118-252T>G	NP_001369732.1:n.3118-252T>G
NM_001382804.1:c.2474T>G	NP_001369733.1:p.Leu825Arg
NM_001382805.1:c.2351T>G	NP_001369734.1:p.Leu784Arg
NM_001382806.1:c.2264T>G	NP_001369735.1:p.Leu755Arg
NM_004448.4:c.3302T>G MANE Select	NP_004439.2:p.Leu1101Arg
NR_110535.2:n.3540T>G