Canonical Allele Identifier: CA399310239

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37883587G>T (hg19) ; chr17:g.39727334G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727334G>T , CM000679.2:g.39727334G>T	GRCh38
NC_000017.10:g.37883587G>T , CM000679.1:g.37883587G>T	GRCh37
NC_000017.9:g.35137113G>T	NCBI36
NG_007503.1:g.44195G>T , LRG_724:g.44195G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3199G>T MANE Select	ENSP00000269571.4:p.Glu1067Ter
ENST00000269571.9:c.3199G>T	ENSP00000269571.4:p.Glu1067Ter
ENST00000406381.6:c.3109G>T	ENSP00000385185.2:p.Glu1037Ter
ENST00000445658.6:c.2371G>T	ENSP00000404047.2:p.Glu791Ter
ENST00000541774.5:c.3154G>T	ENSP00000446466.1:p.Glu1052Ter
ENST00000578373.5:c.*2989G>T	ENSP00000463427.1:n.*2989G>T
ENST00000584450.5:c.3159+331G>T	ENSP00000463714.1:n.3159+331G>T
ENST00000584601.5:c.3109G>T	ENSP00000462438.1:p.Glu1037Ter
NM_001005862.2:c.3109G>T , LRG_724t1:c.3109G>T	NP_001005862.1:p.Glu1037Ter
NM_001289936.1:c.3154G>T , LRG_724t4:c.3154G>T	NP_001276865.1:p.Glu1052Ter
NM_001289937.1:c.3159+331G>T	NP_001276866.1:n.3159+331G>T
NM_004448.3:c.3199G>T , LRG_724t2:c.3199G>T	NP_004439.2:p.Glu1067Ter
NR_110535.1:n.3523G>T
XM_024450641.1:c.3337G>T	XP_024306409.1:p.Glu1113Ter
XM_024450642.1:c.3292G>T	XP_024306410.1:p.Glu1098Ter
XM_024450643.1:c.3247G>T	XP_024306411.1:p.Glu1083Ter
NM_001005862.3:c.3109G>T	NP_001005862.1:p.Glu1037Ter
NM_001289936.2:c.3154G>T	NP_001276865.1:p.Glu1052Ter
NM_001289937.2:c.3159+331G>T	NP_001276866.1:n.3159+331G>T
NM_001382782.1:c.3109G>T	NP_001369711.1:p.Glu1037Ter
NM_001382783.1:c.3109G>T	NP_001369712.1:p.Glu1037Ter
NM_001382784.1:c.3316G>T	NP_001369713.1:p.Glu1106Ter
NM_001382785.1:c.3301G>T	NP_001369714.1:p.Glu1101Ter
NM_001382786.1:c.3280G>T	NP_001369715.1:p.Glu1094Ter
NM_001382787.1:c.3274G>T	NP_001369716.1:p.Glu1092Ter
NM_001382788.1:c.3229G>T	NP_001369717.1:p.Glu1077Ter
NM_001382789.1:c.3220G>T	NP_001369718.1:p.Glu1074Ter
NM_001382790.1:c.3196G>T	NP_001369719.1:p.Glu1066Ter
NM_001382791.1:c.3190G>T	NP_001369720.1:p.Glu1064Ter
NM_001382792.1:c.3163G>T	NP_001369721.1:p.Glu1055Ter
NM_001382793.1:c.3157G>T	NP_001369722.1:p.Glu1053Ter
NM_001382794.1:c.3157G>T	NP_001369723.1:p.Glu1053Ter
NM_001382795.1:c.3151G>T	NP_001369724.1:p.Glu1051Ter
NM_001382796.1:c.3112G>T	NP_001369725.1:p.Glu1038Ter
NM_001382797.1:c.3100G>T	NP_001369726.1:p.Glu1034Ter
NM_001382798.1:c.3043G>T	NP_001369727.1:p.Glu1015Ter
NM_001382799.1:c.3019G>T	NP_001369728.1:p.Glu1007Ter
NM_001382800.1:c.3013G>T	NP_001369729.1:p.Glu1005Ter
NM_001382801.1:c.2995G>T	NP_001369730.1:p.Glu999Ter
NM_001382802.1:c.2941G>T	NP_001369731.1:p.Glu981Ter
NM_001382803.1:c.3117+331G>T	NP_001369732.1:n.3117+331G>T
NM_001382804.1:c.2371G>T	NP_001369733.1:p.Glu791Ter
NM_001382805.1:c.2248G>T	NP_001369734.1:p.Glu750Ter
NM_001382806.1:c.2161G>T	NP_001369735.1:p.Glu721Ter
NM_004448.4:c.3199G>T MANE Select	NP_004439.2:p.Glu1067Ter
NR_110535.2:n.3437G>T