Canonical Allele Identifier: CA399310212

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37883580G>T (hg19) ; chr17:g.39727327G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727327G>T , CM000679.2:g.39727327G>T	GRCh38
NC_000017.10:g.37883580G>T , CM000679.1:g.37883580G>T	GRCh37
NC_000017.9:g.35137106G>T	NCBI36
NG_007503.1:g.44188G>T , LRG_724:g.44188G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3192G>T MANE Select	ENSP00000269571.4:p.Glu1064Asp
ENST00000269571.9:c.3192G>T	ENSP00000269571.4:p.Glu1064Asp
ENST00000406381.6:c.3102G>T	ENSP00000385185.2:p.Glu1034Asp
ENST00000445658.6:c.2364G>T	ENSP00000404047.2:p.Glu788Asp
ENST00000541774.5:c.3147G>T	ENSP00000446466.1:p.Glu1049Asp
ENST00000578373.5:c.*2982G>T	ENSP00000463427.1:n.*2982G>T
ENST00000584450.5:c.3159+324G>T	ENSP00000463714.1:n.3159+324G>T
ENST00000584601.5:c.3102G>T	ENSP00000462438.1:p.Glu1034Asp
NM_001005862.2:c.3102G>T , LRG_724t1:c.3102G>T	NP_001005862.1:p.Glu1034Asp
NM_001289936.1:c.3147G>T , LRG_724t4:c.3147G>T	NP_001276865.1:p.Glu1049Asp
NM_001289937.1:c.3159+324G>T	NP_001276866.1:n.3159+324G>T
NM_004448.3:c.3192G>T , LRG_724t2:c.3192G>T	NP_004439.2:p.Glu1064Asp
NR_110535.1:n.3516G>T
XM_024450641.1:c.3330G>T	XP_024306409.1:p.Glu1110Asp
XM_024450642.1:c.3285G>T	XP_024306410.1:p.Glu1095Asp
XM_024450643.1:c.3240G>T	XP_024306411.1:p.Glu1080Asp
NM_001005862.3:c.3102G>T	NP_001005862.1:p.Glu1034Asp
NM_001289936.2:c.3147G>T	NP_001276865.1:p.Glu1049Asp
NM_001289937.2:c.3159+324G>T	NP_001276866.1:n.3159+324G>T
NM_001382782.1:c.3102G>T	NP_001369711.1:p.Glu1034Asp
NM_001382783.1:c.3102G>T	NP_001369712.1:p.Glu1034Asp
NM_001382784.1:c.3309G>T	NP_001369713.1:p.Glu1103Asp
NM_001382785.1:c.3294G>T	NP_001369714.1:p.Glu1098Asp
NM_001382786.1:c.3273G>T	NP_001369715.1:p.Glu1091Asp
NM_001382787.1:c.3267G>T	NP_001369716.1:p.Glu1089Asp
NM_001382788.1:c.3222G>T	NP_001369717.1:p.Glu1074Asp
NM_001382789.1:c.3213G>T	NP_001369718.1:p.Glu1071Asp
NM_001382790.1:c.3189G>T	NP_001369719.1:p.Glu1063Asp
NM_001382791.1:c.3183G>T	NP_001369720.1:p.Glu1061Asp
NM_001382792.1:c.3156G>T	NP_001369721.1:p.Glu1052Asp
NM_001382793.1:c.3150G>T	NP_001369722.1:p.Glu1050Asp
NM_001382794.1:c.3150G>T	NP_001369723.1:p.Glu1050Asp
NM_001382795.1:c.3144G>T	NP_001369724.1:p.Glu1048Asp
NM_001382796.1:c.3105G>T	NP_001369725.1:p.Glu1035Asp
NM_001382797.1:c.3093G>T	NP_001369726.1:p.Glu1031Asp
NM_001382798.1:c.3036G>T	NP_001369727.1:p.Glu1012Asp
NM_001382799.1:c.3012G>T	NP_001369728.1:p.Glu1004Asp
NM_001382800.1:c.3006G>T	NP_001369729.1:p.Glu1002Asp
NM_001382801.1:c.2988G>T	NP_001369730.1:p.Glu996Asp
NM_001382802.1:c.2934G>T	NP_001369731.1:p.Glu978Asp
NM_001382803.1:c.3117+324G>T	NP_001369732.1:n.3117+324G>T
NM_001382804.1:c.2364G>T	NP_001369733.1:p.Glu788Asp
NM_001382805.1:c.2241G>T	NP_001369734.1:p.Glu747Asp
NM_001382806.1:c.2154G>T	NP_001369735.1:p.Glu718Asp
NM_004448.4:c.3192G>T MANE Select	NP_004439.2:p.Glu1064Asp
NR_110535.2:n.3430G>T