Canonical Allele Identifier: CA399282034

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37868202T>C (hg19) ; chr17:g.39711949T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39711949T>C , CM000679.2:g.39711949T>C	GRCh38
NC_000017.10:g.37868202T>C , CM000679.1:g.37868202T>C	GRCh37
NC_000017.9:g.35121728T>C	NCBI36
NG_007503.1:g.28810T>C , LRG_724:g.28810T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.923T>C MANE Select	ENSP00000269571.4:p.Val308Ala
ENST00000269571.9:c.923T>C	ENSP00000269571.4:p.Val308Ala
ENST00000406381.6:c.833T>C	ENSP00000385185.2:p.Val278Ala
ENST00000445658.6:c.95T>C	ENSP00000404047.2:p.Val32Ala
ENST00000541774.5:c.878T>C	ENSP00000446466.1:p.Val293Ala
ENST00000578199.5:c.833T>C	ENSP00000462808.1:p.Val278Ala
ENST00000578373.5:c.*713T>C	ENSP00000463427.1:n.*713T>C
ENST00000578502.1:c.148T>C
ENST00000582648.5:c.247T>C	ENSP00000462024.1:p.Trp83Arg
ENST00000582788.5:n.412T>C
ENST00000583038.5:n.1615T>C
ENST00000584450.5:c.923T>C	ENSP00000463714.1:p.Val308Ala
ENST00000584601.5:c.833T>C	ENSP00000462438.1:p.Val278Ala
ENST00000584908.5:n.935T>C
NM_001005862.2:c.833T>C , LRG_724t1:c.833T>C	NP_001005862.1:p.Val278Ala
NM_001289936.1:c.878T>C , LRG_724t4:c.878T>C	NP_001276865.1:p.Val293Ala
NM_001289937.1:c.923T>C	NP_001276866.1:p.Val308Ala
NM_001289938.1:c.833T>C , LRG_724t3:c.833T>C	NP_001276867.1:p.Val278Ala
NM_004448.3:c.923T>C , LRG_724t2:c.923T>C	NP_004439.2:p.Val308Ala
NR_110535.1:n.1247T>C
XM_024450641.1:c.1061T>C	XP_024306409.1:p.Val354Ala
XM_024450642.1:c.1016T>C	XP_024306410.1:p.Val339Ala
XM_024450643.1:c.971T>C	XP_024306411.1:p.Val324Ala
NM_001005862.3:c.833T>C	NP_001005862.1:p.Val278Ala
NM_001289936.2:c.878T>C	NP_001276865.1:p.Val293Ala
NM_001289937.2:c.923T>C	NP_001276866.1:p.Val308Ala
NM_001289938.2:c.833T>C	NP_001276867.1:p.Val278Ala
NM_001382782.1:c.833T>C	NP_001369711.1:p.Val278Ala
NM_001382783.1:c.833T>C	NP_001369712.1:p.Val278Ala
NM_001382784.1:c.923T>C	NP_001369713.1:p.Val308Ala
NM_001382785.1:c.923T>C	NP_001369714.1:p.Val308Ala
NM_001382786.1:c.923T>C	NP_001369715.1:p.Val308Ala
NM_001382787.1:c.998T>C	NP_001369716.1:p.Val333Ala
NM_001382788.1:c.923T>C	NP_001369717.1:p.Val308Ala
NM_001382789.1:c.923T>C	NP_001369718.1:p.Val308Ala
NM_001382790.1:c.923T>C	NP_001369719.1:p.Val308Ala
NM_001382791.1:c.914T>C	NP_001369720.1:p.Val305Ala
NM_001382792.1:c.923T>C	NP_001369721.1:p.Val308Ala
NM_001382793.1:c.923T>C	NP_001369722.1:p.Val308Ala
NM_001382794.1:c.923T>C	NP_001369723.1:p.Val308Ala
NM_001382795.1:c.923T>C	NP_001369724.1:p.Val308Ala
NM_001382796.1:c.923T>C	NP_001369725.1:p.Val308Ala
NM_001382797.1:c.923T>C	NP_001369726.1:p.Val308Ala
NM_001382798.1:c.923T>C	NP_001369727.1:p.Val308Ala
NM_001382799.1:c.743T>C	NP_001369728.1:p.Val248Ala
NM_001382800.1:c.923T>C	NP_001369729.1:p.Val308Ala
NM_001382801.1:c.923T>C	NP_001369730.1:p.Val308Ala
NM_001382802.1:c.665T>C	NP_001369731.1:p.Val222Ala
NM_001382803.1:c.923T>C	NP_001369732.1:p.Val308Ala
NM_001382804.1:c.95T>C	NP_001369733.1:p.Val32Ala
NM_001382805.1:c.923T>C	NP_001369734.1:p.Val308Ala
NM_001382806.1:c.923T>C	NP_001369735.1:p.Val308Ala
NM_004448.4:c.923T>C MANE Select	NP_004439.2:p.Val308Ala
NR_110535.2:n.1161T>C