Canonical Allele Identifier: CA499670824

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37880984A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39724731A>C , CM000679.2:g.39724731A>C	GRCh38
NC_000017.10:g.37880984A>C , CM000679.1:g.37880984A>C	GRCh37
NC_000017.9:g.35134510A>C	NCBI36
NG_007503.1:g.41592A>C , LRG_724:g.41592A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.2313A>C MANE Select	ENSP00000269571.4:p.Ala771=
ENST00000269571.9:c.2313A>C	ENSP00000269571.4:p.Ala771=
ENST00000406381.6:c.2223A>C	ENSP00000385185.2:p.Ala741=
ENST00000445658.6:c.1485A>C	ENSP00000404047.2:p.Ala495=
ENST00000541774.5:c.2268A>C	ENSP00000446466.1:p.Ala756=
ENST00000578373.5:c.*2103A>C	ENSP00000463427.1:n.*2103A>C
ENST00000580074.1:c.419A>C
ENST00000583038.5:n.3447A>C
ENST00000584450.5:c.2313A>C	ENSP00000463714.1:p.Ala771=
ENST00000584601.5:c.2223A>C	ENSP00000462438.1:p.Ala741=
NM_001005862.2:c.2223A>C , LRG_724t1:c.2223A>C	NP_001005862.1:p.Ala741=
NM_001289936.1:c.2268A>C , LRG_724t4:c.2268A>C	NP_001276865.1:p.Ala756=
NM_001289937.1:c.2313A>C	NP_001276866.1:p.Ala771=
NM_004448.3:c.2313A>C , LRG_724t2:c.2313A>C	NP_004439.2:p.Ala771=
NR_110535.1:n.2637A>C
XM_024450641.1:c.2451A>C	XP_024306409.1:p.Ala817=
XM_024450642.1:c.2406A>C	XP_024306410.1:p.Ala802=
XM_024450643.1:c.2361A>C	XP_024306411.1:p.Ala787=
NM_001005862.3:c.2223A>C	NP_001005862.1:p.Ala741=
NM_001289936.2:c.2268A>C	NP_001276865.1:p.Ala756=
NM_001289937.2:c.2313A>C	NP_001276866.1:p.Ala771=
NM_001382782.1:c.2223A>C	NP_001369711.1:p.Ala741=
NM_001382783.1:c.2223A>C	NP_001369712.1:p.Ala741=
NM_001382784.1:c.2430A>C	NP_001369713.1:p.Ala810=
NM_001382785.1:c.2415A>C	NP_001369714.1:p.Ala805=
NM_001382786.1:c.2394A>C	NP_001369715.1:p.Ala798=
NM_001382787.1:c.2388A>C	NP_001369716.1:p.Ala796=
NM_001382788.1:c.2343A>C	NP_001369717.1:p.Ala781=
NM_001382789.1:c.2334A>C	NP_001369718.1:p.Ala778=
NM_001382790.1:c.2310A>C	NP_001369719.1:p.Ala770=
NM_001382791.1:c.2304A>C	NP_001369720.1:p.Ala768=
NM_001382792.1:c.2277A>C	NP_001369721.1:p.Ala759=
NM_001382793.1:c.2271A>C	NP_001369722.1:p.Ala757=
NM_001382794.1:c.2271A>C	NP_001369723.1:p.Ala757=
NM_001382795.1:c.2265A>C	NP_001369724.1:p.Ala755=
NM_001382796.1:c.2313A>C	NP_001369725.1:p.Ala771=
NM_001382797.1:c.2214A>C	NP_001369726.1:p.Ala738=
NM_001382798.1:c.2313A>C	NP_001369727.1:p.Ala771=
NM_001382799.1:c.2133A>C	NP_001369728.1:p.Ala711=
NM_001382800.1:c.2308-318A>C	NP_001369729.1:n.2308-318A>C
NM_001382801.1:c.2265A>C	NP_001369730.1:p.Ala755=
NM_001382802.1:c.2055A>C	NP_001369731.1:p.Ala685=
NM_001382803.1:c.2271A>C	NP_001369732.1:p.Ala757=
NM_001382804.1:c.1485A>C	NP_001369733.1:p.Ala495=
NM_001382805.1:c.2208+1071A>C	NP_001369734.1:n.2208+1071A>C
NM_001382806.1:c.1275A>C	NP_001369735.1:p.Ala425=
NM_004448.4:c.2313A>C MANE Select	NP_004439.2:p.Ala771=
NR_110535.2:n.2551A>C