Canonical Allele Identifier: CA399303289

Gene: ERBB2

Linked Data

• dbSNP Id: rs2145850719
• MyVariant Identifiers: chr17:g.37881072A>G (hg19) ; chr17:g.39724819A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39724819A>G , CM000679.2:g.39724819A>G	GRCh38
NC_000017.10:g.37881072A>G , CM000679.1:g.37881072A>G	GRCh37
NC_000017.9:g.35134598A>G	NCBI36
NG_007503.1:g.41680A>G , LRG_724:g.41680A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.2401A>G MANE Select	ENSP00000269571.4:p.Met801Val
ENST00000269571.9:c.2401A>G	ENSP00000269571.4:p.Met801Val
ENST00000406381.6:c.2311A>G	ENSP00000385185.2:p.Met771Val
ENST00000445658.6:c.1573A>G	ENSP00000404047.2:p.Met525Val
ENST00000541774.5:c.2356A>G	ENSP00000446466.1:p.Met786Val
ENST00000578373.5:c.*2191A>G	ENSP00000463427.1:n.*2191A>G
ENST00000580074.1:c.507A>G
ENST00000583038.5:n.3535A>G
ENST00000584450.5:c.2401A>G	ENSP00000463714.1:p.Met801Val
ENST00000584601.5:c.2311A>G	ENSP00000462438.1:p.Met771Val
NM_001005862.2:c.2311A>G , LRG_724t1:c.2311A>G	NP_001005862.1:p.Met771Val
NM_001289936.1:c.2356A>G , LRG_724t4:c.2356A>G	NP_001276865.1:p.Met786Val
NM_001289937.1:c.2401A>G	NP_001276866.1:p.Met801Val
NM_004448.3:c.2401A>G , LRG_724t2:c.2401A>G	NP_004439.2:p.Met801Val
NR_110535.1:n.2725A>G
XM_024450641.1:c.2539A>G	XP_024306409.1:p.Met847Val
XM_024450642.1:c.2494A>G	XP_024306410.1:p.Met832Val
XM_024450643.1:c.2449A>G	XP_024306411.1:p.Met817Val
NM_001005862.3:c.2311A>G	NP_001005862.1:p.Met771Val
NM_001289936.2:c.2356A>G	NP_001276865.1:p.Met786Val
NM_001289937.2:c.2401A>G	NP_001276866.1:p.Met801Val
NM_001382782.1:c.2311A>G	NP_001369711.1:p.Met771Val
NM_001382783.1:c.2311A>G	NP_001369712.1:p.Met771Val
NM_001382784.1:c.2518A>G	NP_001369713.1:p.Met840Val
NM_001382785.1:c.2503A>G	NP_001369714.1:p.Met835Val
NM_001382786.1:c.2482A>G	NP_001369715.1:p.Met828Val
NM_001382787.1:c.2476A>G	NP_001369716.1:p.Met826Val
NM_001382788.1:c.2431A>G	NP_001369717.1:p.Met811Val
NM_001382789.1:c.2422A>G	NP_001369718.1:p.Met808Val
NM_001382790.1:c.2398A>G	NP_001369719.1:p.Met800Val
NM_001382791.1:c.2392A>G	NP_001369720.1:p.Met798Val
NM_001382792.1:c.2365A>G	NP_001369721.1:p.Met789Val
NM_001382793.1:c.2359A>G	NP_001369722.1:p.Met787Val
NM_001382794.1:c.2359A>G	NP_001369723.1:p.Met787Val
NM_001382795.1:c.2353A>G	NP_001369724.1:p.Met785Val
NM_001382796.1:c.2401A>G	NP_001369725.1:p.Met801Val
NM_001382797.1:c.2302A>G	NP_001369726.1:p.Met768Val
NM_001382798.1:c.2401A>G	NP_001369727.1:p.Met801Val
NM_001382799.1:c.2221A>G	NP_001369728.1:p.Met741Val
NM_001382800.1:c.2308-230A>G	NP_001369729.1:n.2308-230A>G
NM_001382801.1:c.2353A>G	NP_001369730.1:p.Met785Val
NM_001382802.1:c.2143A>G	NP_001369731.1:p.Met715Val
NM_001382803.1:c.2359A>G	NP_001369732.1:p.Met787Val
NM_001382804.1:c.1573A>G	NP_001369733.1:p.Met525Val
NM_001382805.1:c.2208+1159A>G	NP_001369734.1:n.2208+1159A>G
NM_001382806.1:c.1363A>G	NP_001369735.1:p.Met455Val
NM_004448.4:c.2401A>G MANE Select	NP_004439.2:p.Met801Val
NR_110535.2:n.2639A>G