Canonical Allele Identifier: CA399312538

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143251451
• MyVariant Identifiers: chr17:g.37883718G>T (hg19) ; chr17:g.39727465G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727465G>T , CM000679.2:g.39727465G>T	GRCh38
NC_000017.10:g.37883718G>T , CM000679.1:g.37883718G>T	GRCh37
NC_000017.9:g.35137244G>T	NCBI36
NG_007503.1:g.44326G>T , LRG_724:g.44326G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3330G>T MANE Select	ENSP00000269571.4:p.Gln1110His
ENST00000269571.9:c.3330G>T	ENSP00000269571.4:p.Gln1110His
ENST00000406381.6:c.3240G>T	ENSP00000385185.2:p.Gln1080His
ENST00000445658.6:c.2502G>T	ENSP00000404047.2:p.Gln834His
ENST00000541774.5:c.3285G>T	ENSP00000446466.1:p.Gln1095His
ENST00000578373.5:c.*3120G>T	ENSP00000463427.1:n.*3120G>T
ENST00000584450.5:c.3160-224G>T	ENSP00000463714.1:n.3160-224G>T
ENST00000584601.5:c.3240G>T	ENSP00000462438.1:p.Gln1080His
NM_001005862.2:c.3240G>T , LRG_724t1:c.3240G>T	NP_001005862.1:p.Gln1080His
NM_001289936.1:c.3285G>T , LRG_724t4:c.3285G>T	NP_001276865.1:p.Gln1095His
NM_001289937.1:c.3160-224G>T	NP_001276866.1:n.3160-224G>T
NM_004448.3:c.3330G>T , LRG_724t2:c.3330G>T	NP_004439.2:p.Gln1110His
NR_110535.1:n.3654G>T
XM_024450641.1:c.3468G>T	XP_024306409.1:p.Gln1156His
XM_024450642.1:c.3423G>T	XP_024306410.1:p.Gln1141His
XM_024450643.1:c.3378G>T	XP_024306411.1:p.Gln1126His
NM_001005862.3:c.3240G>T	NP_001005862.1:p.Gln1080His
NM_001289936.2:c.3285G>T	NP_001276865.1:p.Gln1095His
NM_001289937.2:c.3160-224G>T	NP_001276866.1:n.3160-224G>T
NM_001382782.1:c.3240G>T	NP_001369711.1:p.Gln1080His
NM_001382783.1:c.3240G>T	NP_001369712.1:p.Gln1080His
NM_001382784.1:c.3447G>T	NP_001369713.1:p.Gln1149His
NM_001382785.1:c.3432G>T	NP_001369714.1:p.Gln1144His
NM_001382786.1:c.3411G>T	NP_001369715.1:p.Gln1137His
NM_001382787.1:c.3405G>T	NP_001369716.1:p.Gln1135His
NM_001382788.1:c.3360G>T	NP_001369717.1:p.Gln1120His
NM_001382789.1:c.3351G>T	NP_001369718.1:p.Gln1117His
NM_001382790.1:c.3327G>T	NP_001369719.1:p.Gln1109His
NM_001382791.1:c.3321G>T	NP_001369720.1:p.Gln1107His
NM_001382792.1:c.3294G>T	NP_001369721.1:p.Gln1098His
NM_001382793.1:c.3288G>T	NP_001369722.1:p.Gln1096His
NM_001382794.1:c.3288G>T	NP_001369723.1:p.Gln1096His
NM_001382795.1:c.3282G>T	NP_001369724.1:p.Gln1094His
NM_001382796.1:c.3243G>T	NP_001369725.1:p.Gln1081His
NM_001382797.1:c.3231G>T	NP_001369726.1:p.Gln1077His
NM_001382798.1:c.3174G>T	NP_001369727.1:p.Gln1058His
NM_001382799.1:c.3150G>T	NP_001369728.1:p.Gln1050His
NM_001382800.1:c.3144G>T	NP_001369729.1:p.Gln1048His
NM_001382801.1:c.3126G>T	NP_001369730.1:p.Gln1042His
NM_001382802.1:c.3072G>T	NP_001369731.1:p.Gln1024His
NM_001382803.1:c.3118-224G>T	NP_001369732.1:n.3118-224G>T
NM_001382804.1:c.2502G>T	NP_001369733.1:p.Gln834His
NM_001382805.1:c.2379G>T	NP_001369734.1:p.Gln793His
NM_001382806.1:c.2292G>T	NP_001369735.1:p.Gln764His
NM_004448.4:c.3330G>T MANE Select	NP_004439.2:p.Gln1110His
NR_110535.2:n.3568G>T