Canonical Allele Identifier: CA399314296

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37884183C>A (hg19) ; chr17:g.39727930C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727930C>A , CM000679.2:g.39727930C>A	GRCh38
NC_000017.10:g.37884183C>A , CM000679.1:g.37884183C>A	GRCh37
NC_000017.9:g.35137709C>A	NCBI36
NG_007503.1:g.44791C>A , LRG_724:g.44791C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3654C>A MANE Select	ENSP00000269571.4:p.Asp1218Glu
ENST00000269571.9:c.3654C>A	ENSP00000269571.4:p.Asp1218Glu
ENST00000406381.6:c.3564C>A	ENSP00000385185.2:p.Asp1188Glu
ENST00000445658.6:c.2826C>A	ENSP00000404047.2:p.Asp942Glu
ENST00000541774.5:c.3609C>A	ENSP00000446466.1:p.Asp1203Glu
ENST00000578373.5:c.*3444C>A	ENSP00000463427.1:n.*3444C>A
ENST00000584450.5:c.*233C>A	ENSP00000463714.1:n.*233C>A
ENST00000584601.5:c.3564C>A	ENSP00000462438.1:p.Asp1188Glu
NM_001005862.2:c.3564C>A , LRG_724t1:c.3564C>A	NP_001005862.1:p.Asp1188Glu
NM_001289936.1:c.3609C>A , LRG_724t4:c.3609C>A	NP_001276865.1:p.Asp1203Glu
NM_001289937.1:c.*233C>A	NP_001276866.1:n.*233C>A
NM_004448.3:c.3654C>A , LRG_724t2:c.3654C>A	NP_004439.2:p.Asp1218Glu
NR_110535.1:n.3978C>A
XM_024450641.1:c.3792C>A	XP_024306409.1:p.Asp1264Glu
XM_024450642.1:c.3747C>A	XP_024306410.1:p.Asp1249Glu
XM_024450643.1:c.3702C>A	XP_024306411.1:p.Asp1234Glu
NM_001005862.3:c.3564C>A	NP_001005862.1:p.Asp1188Glu
NM_001289936.2:c.3609C>A	NP_001276865.1:p.Asp1203Glu
NM_001289937.2:c.*233C>A	NP_001276866.1:n.*233C>A
NM_001382782.1:c.3564C>A	NP_001369711.1:p.Asp1188Glu
NM_001382783.1:c.3564C>A	NP_001369712.1:p.Asp1188Glu
NM_001382784.1:c.3771C>A	NP_001369713.1:p.Asp1257Glu
NM_001382785.1:c.3756C>A	NP_001369714.1:p.Asp1252Glu
NM_001382786.1:c.3735C>A	NP_001369715.1:p.Asp1245Glu
NM_001382787.1:c.3729C>A	NP_001369716.1:p.Asp1243Glu
NM_001382788.1:c.3684C>A	NP_001369717.1:p.Asp1228Glu
NM_001382789.1:c.3675C>A	NP_001369718.1:p.Asp1225Glu
NM_001382790.1:c.3651C>A	NP_001369719.1:p.Asp1217Glu
NM_001382791.1:c.3645C>A	NP_001369720.1:p.Asp1215Glu
NM_001382792.1:c.3618C>A	NP_001369721.1:p.Asp1206Glu
NM_001382793.1:c.3612C>A	NP_001369722.1:p.Asp1204Glu
NM_001382794.1:c.3612C>A	NP_001369723.1:p.Asp1204Glu
NM_001382795.1:c.3606C>A	NP_001369724.1:p.Asp1202Glu
NM_001382796.1:c.3567C>A	NP_001369725.1:p.Asp1189Glu
NM_001382797.1:c.3555C>A	NP_001369726.1:p.Asp1185Glu
NM_001382798.1:c.3498C>A	NP_001369727.1:p.Asp1166Glu
NM_001382799.1:c.3474C>A	NP_001369728.1:p.Asp1158Glu
NM_001382800.1:c.3468C>A	NP_001369729.1:p.Asp1156Glu
NM_001382801.1:c.3450C>A	NP_001369730.1:p.Asp1150Glu
NM_001382802.1:c.3396C>A	NP_001369731.1:p.Asp1132Glu
NM_001382803.1:c.*233C>A	NP_001369732.1:n.*233C>A
NM_001382804.1:c.2826C>A	NP_001369733.1:p.Asp942Glu
NM_001382805.1:c.2703C>A	NP_001369734.1:p.Asp901Glu
NM_001382806.1:c.2616C>A	NP_001369735.1:p.Asp872Glu
NM_004448.4:c.3654C>A MANE Select	NP_004439.2:p.Asp1218Glu
NR_110535.2:n.3892C>A