Canonical Allele Identifier: CA399302686

Gene: ERBB2

Linked Data

• dbSNP Id: rs2145828271
• MyVariant Identifiers: chr17:g.37880262A>T (hg19) ; chr17:g.39724009A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39724009A>T , CM000679.2:g.39724009A>T	GRCh38
NC_000017.10:g.37880262A>T , CM000679.1:g.37880262A>T	GRCh37
NC_000017.9:g.35133788A>T	NCBI36
NG_007503.1:g.40870A>T , LRG_724:g.40870A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000269571.10:c.2306A>T MANE Select	ENSP00000269571.4:p.Asp769Val
ENST00000269571.9:c.2306A>T	ENSP00000269571.4:p.Asp769Val
ENST00000406381.6:c.2216A>T	ENSP00000385185.2:p.Asp739Val
ENST00000445658.6:c.1478A>T	ENSP00000404047.2:p.Asp493Val
ENST00000541774.5:c.2261A>T	ENSP00000446466.1:p.Asp754Val
ENST00000578373.5:c.*2096A>T	ENSP00000463427.1:n.*2096A>T
ENST00000580074.1:c.412A>T
ENST00000583038.5:n.3440A>T
ENST00000584450.5:c.2306A>T	ENSP00000463714.1:p.Asp769Val
ENST00000584601.5:c.2216A>T	ENSP00000462438.1:p.Asp739Val
NM_001005862.2:c.2216A>T , LRG_724t1:c.2216A>T	NP_001005862.1:p.Asp739Val
NM_001289936.1:c.2261A>T , LRG_724t4:c.2261A>T	NP_001276865.1:p.Asp754Val
NM_001289937.1:c.2306A>T	NP_001276866.1:p.Asp769Val
NM_004448.3:c.2306A>T , LRG_724t2:c.2306A>T	NP_004439.2:p.Asp769Val
NR_110535.1:n.2630A>T
XM_024450641.1:c.2444A>T	XP_024306409.1:p.Asp815Val
XM_024450642.1:c.2399A>T	XP_024306410.1:p.Asp800Val
XM_024450643.1:c.2354A>T	XP_024306411.1:p.Asp785Val
NM_001005862.3:c.2216A>T	NP_001005862.1:p.Asp739Val
NM_001289936.2:c.2261A>T	NP_001276865.1:p.Asp754Val
NM_001289937.2:c.2306A>T	NP_001276866.1:p.Asp769Val
NM_001382782.1:c.2216A>T	NP_001369711.1:p.Asp739Val
NM_001382783.1:c.2216A>T	NP_001369712.1:p.Asp739Val
NM_001382784.1:c.2423A>T	NP_001369713.1:p.Asp808Val
NM_001382785.1:c.2408A>T	NP_001369714.1:p.Asp803Val
NM_001382786.1:c.2387A>T	NP_001369715.1:p.Asp796Val
NM_001382787.1:c.2381A>T	NP_001369716.1:p.Asp794Val
NM_001382788.1:c.2336A>T	NP_001369717.1:p.Asp779Val
NM_001382789.1:c.2327A>T	NP_001369718.1:p.Asp776Val
NM_001382790.1:c.2303A>T	NP_001369719.1:p.Asp768Val
NM_001382791.1:c.2297A>T	NP_001369720.1:p.Asp766Val
NM_001382792.1:c.2270A>T	NP_001369721.1:p.Asp757Val
NM_001382793.1:c.2264A>T	NP_001369722.1:p.Asp755Val
NM_001382794.1:c.2264A>T	NP_001369723.1:p.Asp755Val
NM_001382795.1:c.2258A>T	NP_001369724.1:p.Asp753Val
NM_001382796.1:c.2306A>T	NP_001369725.1:p.Asp769Val
NM_001382797.1:c.2208+349A>T	NP_001369726.1:n.2208+349A>T
NM_001382798.1:c.2306A>T	NP_001369727.1:p.Asp769Val
NM_001382799.1:c.2126A>T	NP_001369728.1:p.Asp709Val
NM_001382800.1:c.2306A>T	NP_001369729.1:p.Asp769Val
NM_001382801.1:c.2258A>T	NP_001369730.1:p.Asp753Val
NM_001382802.1:c.2048A>T	NP_001369731.1:p.Asp683Val
NM_001382803.1:c.2264A>T	NP_001369732.1:p.Asp755Val
NM_001382804.1:c.1478A>T	NP_001369733.1:p.Asp493Val
NM_001382805.1:c.2208+349A>T	NP_001369734.1:n.2208+349A>T
NM_001382806.1:c.1268A>T	NP_001369735.1:p.Asp423Val
NM_004448.4:c.2306A>T MANE Select	NP_004439.2:p.Asp769Val
NR_110535.2:n.2544A>T