Canonical Allele Identifier: CA399304372

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37881342A>T (hg19) ; chr17:g.39725089A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39725089A>T , CM000679.2:g.39725089A>T	GRCh38
NC_000017.10:g.37881342A>T , CM000679.1:g.37881342A>T	GRCh37
NC_000017.9:g.35134868A>T	NCBI36
NG_007503.1:g.41950A>T , LRG_724:g.41950A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.2534A>T MANE Select	ENSP00000269571.4:p.Asp845Val
ENST00000269571.9:c.2534A>T	ENSP00000269571.4:p.Asp845Val
ENST00000406381.6:c.2444A>T	ENSP00000385185.2:p.Asp815Val
ENST00000445658.6:c.1706A>T	ENSP00000404047.2:p.Asp569Val
ENST00000541774.5:c.2489A>T	ENSP00000446466.1:p.Asp830Val
ENST00000578373.5:c.*2324A>T	ENSP00000463427.1:n.*2324A>T
ENST00000580074.1:c.640A>T
ENST00000583038.5:n.3668A>T
ENST00000584450.5:c.2534A>T	ENSP00000463714.1:p.Asp845Val
ENST00000584601.5:c.2444A>T	ENSP00000462438.1:p.Asp815Val
NM_001005862.2:c.2444A>T , LRG_724t1:c.2444A>T	NP_001005862.1:p.Asp815Val
NM_001289936.1:c.2489A>T , LRG_724t4:c.2489A>T	NP_001276865.1:p.Asp830Val
NM_001289937.1:c.2534A>T	NP_001276866.1:p.Asp845Val
NM_004448.3:c.2534A>T , LRG_724t2:c.2534A>T	NP_004439.2:p.Asp845Val
NR_110535.1:n.2858A>T
XM_024450641.1:c.2672A>T	XP_024306409.1:p.Asp891Val
XM_024450642.1:c.2627A>T	XP_024306410.1:p.Asp876Val
XM_024450643.1:c.2582A>T	XP_024306411.1:p.Asp861Val
NM_001005862.3:c.2444A>T	NP_001005862.1:p.Asp815Val
NM_001289936.2:c.2489A>T	NP_001276865.1:p.Asp830Val
NM_001289937.2:c.2534A>T	NP_001276866.1:p.Asp845Val
NM_001382782.1:c.2444A>T	NP_001369711.1:p.Asp815Val
NM_001382783.1:c.2444A>T	NP_001369712.1:p.Asp815Val
NM_001382784.1:c.2651A>T	NP_001369713.1:p.Asp884Val
NM_001382785.1:c.2636A>T	NP_001369714.1:p.Asp879Val
NM_001382786.1:c.2615A>T	NP_001369715.1:p.Asp872Val
NM_001382787.1:c.2609A>T	NP_001369716.1:p.Asp870Val
NM_001382788.1:c.2564A>T	NP_001369717.1:p.Asp855Val
NM_001382789.1:c.2555A>T	NP_001369718.1:p.Asp852Val
NM_001382790.1:c.2531A>T	NP_001369719.1:p.Asp844Val
NM_001382791.1:c.2525A>T	NP_001369720.1:p.Asp842Val
NM_001382792.1:c.2498A>T	NP_001369721.1:p.Asp833Val
NM_001382793.1:c.2492A>T	NP_001369722.1:p.Asp831Val
NM_001382794.1:c.2492A>T	NP_001369723.1:p.Asp831Val
NM_001382795.1:c.2486A>T	NP_001369724.1:p.Asp829Val
NM_001382796.1:c.2534A>T	NP_001369725.1:p.Asp845Val
NM_001382797.1:c.2435A>T	NP_001369726.1:p.Asp812Val
NM_001382798.1:c.2493+178A>T	NP_001369727.1:n.2493+178A>T
NM_001382799.1:c.2354A>T	NP_001369728.1:p.Asp785Val
NM_001382800.1:c.2348A>T	NP_001369729.1:p.Asp783Val
NM_001382801.1:c.2445+178A>T	NP_001369730.1:n.2445+178A>T
NM_001382802.1:c.2276A>T	NP_001369731.1:p.Asp759Val
NM_001382803.1:c.2492A>T	NP_001369732.1:p.Asp831Val
NM_001382804.1:c.1706A>T	NP_001369733.1:p.Asp569Val
NM_001382805.1:c.2208+1429A>T	NP_001369734.1:n.2208+1429A>T
NM_001382806.1:c.1496A>T	NP_001369735.1:p.Asp499Val
NM_004448.4:c.2534A>T MANE Select	NP_004439.2:p.Asp845Val
NR_110535.2:n.2772A>T