Canonical Allele Identifier: CA399304410

Gene: ERBB2

Linked Data

• dbSNP Id: rs2145863871
• MyVariant Identifiers: chr17:g.37881348C>T (hg19) ; chr17:g.39725095C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39725095C>T , CM000679.2:g.39725095C>T	GRCh38
NC_000017.10:g.37881348C>T , CM000679.1:g.37881348C>T	GRCh37
NC_000017.9:g.35134874C>T	NCBI36
NG_007503.1:g.41956C>T , LRG_724:g.41956C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.2540C>T MANE Select	ENSP00000269571.4:p.Ala847Val
ENST00000269571.9:c.2540C>T	ENSP00000269571.4:p.Ala847Val
ENST00000406381.6:c.2450C>T	ENSP00000385185.2:p.Ala817Val
ENST00000445658.6:c.1712C>T	ENSP00000404047.2:p.Ala571Val
ENST00000541774.5:c.2495C>T	ENSP00000446466.1:p.Ala832Val
ENST00000578373.5:c.*2330C>T	ENSP00000463427.1:n.*2330C>T
ENST00000580074.1:c.646C>T
ENST00000583038.5:n.3674C>T
ENST00000584450.5:c.2540C>T	ENSP00000463714.1:p.Ala847Val
ENST00000584601.5:c.2450C>T	ENSP00000462438.1:p.Ala817Val
NM_001005862.2:c.2450C>T , LRG_724t1:c.2450C>T	NP_001005862.1:p.Ala817Val
NM_001289936.1:c.2495C>T , LRG_724t4:c.2495C>T	NP_001276865.1:p.Ala832Val
NM_001289937.1:c.2540C>T	NP_001276866.1:p.Ala847Val
NM_004448.3:c.2540C>T , LRG_724t2:c.2540C>T	NP_004439.2:p.Ala847Val
NR_110535.1:n.2864C>T
XM_024450641.1:c.2678C>T	XP_024306409.1:p.Ala893Val
XM_024450642.1:c.2633C>T	XP_024306410.1:p.Ala878Val
XM_024450643.1:c.2588C>T	XP_024306411.1:p.Ala863Val
NM_001005862.3:c.2450C>T	NP_001005862.1:p.Ala817Val
NM_001289936.2:c.2495C>T	NP_001276865.1:p.Ala832Val
NM_001289937.2:c.2540C>T	NP_001276866.1:p.Ala847Val
NM_001382782.1:c.2450C>T	NP_001369711.1:p.Ala817Val
NM_001382783.1:c.2450C>T	NP_001369712.1:p.Ala817Val
NM_001382784.1:c.2657C>T	NP_001369713.1:p.Ala886Val
NM_001382785.1:c.2642C>T	NP_001369714.1:p.Ala881Val
NM_001382786.1:c.2621C>T	NP_001369715.1:p.Ala874Val
NM_001382787.1:c.2615C>T	NP_001369716.1:p.Ala872Val
NM_001382788.1:c.2570C>T	NP_001369717.1:p.Ala857Val
NM_001382789.1:c.2561C>T	NP_001369718.1:p.Ala854Val
NM_001382790.1:c.2537C>T	NP_001369719.1:p.Ala846Val
NM_001382791.1:c.2531C>T	NP_001369720.1:p.Ala844Val
NM_001382792.1:c.2504C>T	NP_001369721.1:p.Ala835Val
NM_001382793.1:c.2498C>T	NP_001369722.1:p.Ala833Val
NM_001382794.1:c.2498C>T	NP_001369723.1:p.Ala833Val
NM_001382795.1:c.2492C>T	NP_001369724.1:p.Ala831Val
NM_001382796.1:c.2540C>T	NP_001369725.1:p.Ala847Val
NM_001382797.1:c.2441C>T	NP_001369726.1:p.Ala814Val
NM_001382798.1:c.2493+184C>T	NP_001369727.1:n.2493+184C>T
NM_001382799.1:c.2360C>T	NP_001369728.1:p.Ala787Val
NM_001382800.1:c.2354C>T	NP_001369729.1:p.Ala785Val
NM_001382801.1:c.2445+184C>T	NP_001369730.1:n.2445+184C>T
NM_001382802.1:c.2282C>T	NP_001369731.1:p.Ala761Val
NM_001382803.1:c.2498C>T	NP_001369732.1:p.Ala833Val
NM_001382804.1:c.1712C>T	NP_001369733.1:p.Ala571Val
NM_001382805.1:c.2208+1435C>T	NP_001369734.1:n.2208+1435C>T
NM_001382806.1:c.1502C>T	NP_001369735.1:p.Ala501Val
NM_004448.4:c.2540C>T MANE Select	NP_004439.2:p.Ala847Val
NR_110535.2:n.2778C>T