Canonical Allele Identifier: CA499890128

Gene: ERBB2

Linked Data

• dbSNP Id: rs2145864490
• MyVariant Identifiers: chr17:g.37881361G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39725108G>A , CM000679.2:g.39725108G>A	GRCh38
NC_000017.10:g.37881361G>A , CM000679.1:g.37881361G>A	GRCh37
NC_000017.9:g.35134887G>A	NCBI36
NG_007503.1:g.41969G>A , LRG_724:g.41969G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.2553G>A MANE Select	ENSP00000269571.4:p.Val851=
ENST00000269571.9:c.2553G>A	ENSP00000269571.4:p.Val851=
ENST00000406381.6:c.2463G>A	ENSP00000385185.2:p.Val821=
ENST00000445658.6:c.1725G>A	ENSP00000404047.2:p.Val575=
ENST00000541774.5:c.2508G>A	ENSP00000446466.1:p.Val836=
ENST00000578373.5:c.*2343G>A	ENSP00000463427.1:n.*2343G>A
ENST00000580074.1:c.659G>A
ENST00000583038.5:n.3687G>A
ENST00000584450.5:c.2553G>A	ENSP00000463714.1:p.Val851=
ENST00000584601.5:c.2463G>A	ENSP00000462438.1:p.Val821=
NM_001005862.2:c.2463G>A , LRG_724t1:c.2463G>A	NP_001005862.1:p.Val821=
NM_001289936.1:c.2508G>A , LRG_724t4:c.2508G>A	NP_001276865.1:p.Val836=
NM_001289937.1:c.2553G>A	NP_001276866.1:p.Val851=
NM_004448.3:c.2553G>A , LRG_724t2:c.2553G>A	NP_004439.2:p.Val851=
NR_110535.1:n.2877G>A
XM_024450641.1:c.2691G>A	XP_024306409.1:p.Val897=
XM_024450642.1:c.2646G>A	XP_024306410.1:p.Val882=
XM_024450643.1:c.2601G>A	XP_024306411.1:p.Val867=
NM_001005862.3:c.2463G>A	NP_001005862.1:p.Val821=
NM_001289936.2:c.2508G>A	NP_001276865.1:p.Val836=
NM_001289937.2:c.2553G>A	NP_001276866.1:p.Val851=
NM_001382782.1:c.2463G>A	NP_001369711.1:p.Val821=
NM_001382783.1:c.2463G>A	NP_001369712.1:p.Val821=
NM_001382784.1:c.2670G>A	NP_001369713.1:p.Val890=
NM_001382785.1:c.2655G>A	NP_001369714.1:p.Val885=
NM_001382786.1:c.2634G>A	NP_001369715.1:p.Val878=
NM_001382787.1:c.2628G>A	NP_001369716.1:p.Val876=
NM_001382788.1:c.2583G>A	NP_001369717.1:p.Val861=
NM_001382789.1:c.2574G>A	NP_001369718.1:p.Val858=
NM_001382790.1:c.2550G>A	NP_001369719.1:p.Val850=
NM_001382791.1:c.2544G>A	NP_001369720.1:p.Val848=
NM_001382792.1:c.2517G>A	NP_001369721.1:p.Val839=
NM_001382793.1:c.2511G>A	NP_001369722.1:p.Val837=
NM_001382794.1:c.2511G>A	NP_001369723.1:p.Val837=
NM_001382795.1:c.2505G>A	NP_001369724.1:p.Val835=
NM_001382796.1:c.2553G>A	NP_001369725.1:p.Val851=
NM_001382797.1:c.2454G>A	NP_001369726.1:p.Val818=
NM_001382798.1:c.2493+197G>A	NP_001369727.1:n.2493+197G>A
NM_001382799.1:c.2373G>A	NP_001369728.1:p.Val791=
NM_001382800.1:c.2367G>A	NP_001369729.1:p.Val789=
NM_001382801.1:c.2445+197G>A	NP_001369730.1:n.2445+197G>A
NM_001382802.1:c.2295G>A	NP_001369731.1:p.Val765=
NM_001382803.1:c.2511G>A	NP_001369732.1:p.Val837=
NM_001382804.1:c.1725G>A	NP_001369733.1:p.Val575=
NM_001382805.1:c.2208+1448G>A	NP_001369734.1:n.2208+1448G>A
NM_001382806.1:c.1515G>A	NP_001369735.1:p.Val505=
NM_004448.4:c.2553G>A MANE Select	NP_004439.2:p.Val851=
NR_110535.2:n.2791G>A