Canonical Allele Identifier: CA499890138

Gene: ERBB2

Linked Data

• dbSNP Id: rs2145864696
• MyVariant Identifiers: chr17:g.37881367C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39725114C>A , CM000679.2:g.39725114C>A	GRCh38
NC_000017.10:g.37881367C>A , CM000679.1:g.37881367C>A	GRCh37
NC_000017.9:g.35134893C>A	NCBI36
NG_007503.1:g.41975C>A , LRG_724:g.41975C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.2559C>A MANE Select	ENSP00000269571.4:p.Val853=
ENST00000269571.9:c.2559C>A	ENSP00000269571.4:p.Val853=
ENST00000406381.6:c.2469C>A	ENSP00000385185.2:p.Val823=
ENST00000445658.6:c.1731C>A	ENSP00000404047.2:p.Val577=
ENST00000541774.5:c.2514C>A	ENSP00000446466.1:p.Val838=
ENST00000578373.5:c.*2349C>A	ENSP00000463427.1:n.*2349C>A
ENST00000580074.1:c.665C>A
ENST00000583038.5:n.3693C>A
ENST00000584450.5:c.2559C>A	ENSP00000463714.1:p.Val853=
ENST00000584601.5:c.2469C>A	ENSP00000462438.1:p.Val823=
NM_001005862.2:c.2469C>A , LRG_724t1:c.2469C>A	NP_001005862.1:p.Val823=
NM_001289936.1:c.2514C>A , LRG_724t4:c.2514C>A	NP_001276865.1:p.Val838=
NM_001289937.1:c.2559C>A	NP_001276866.1:p.Val853=
NM_004448.3:c.2559C>A , LRG_724t2:c.2559C>A	NP_004439.2:p.Val853=
NR_110535.1:n.2883C>A
XM_024450641.1:c.2697C>A	XP_024306409.1:p.Val899=
XM_024450642.1:c.2652C>A	XP_024306410.1:p.Val884=
XM_024450643.1:c.2607C>A	XP_024306411.1:p.Val869=
NM_001005862.3:c.2469C>A	NP_001005862.1:p.Val823=
NM_001289936.2:c.2514C>A	NP_001276865.1:p.Val838=
NM_001289937.2:c.2559C>A	NP_001276866.1:p.Val853=
NM_001382782.1:c.2469C>A	NP_001369711.1:p.Val823=
NM_001382783.1:c.2469C>A	NP_001369712.1:p.Val823=
NM_001382784.1:c.2676C>A	NP_001369713.1:p.Val892=
NM_001382785.1:c.2661C>A	NP_001369714.1:p.Val887=
NM_001382786.1:c.2640C>A	NP_001369715.1:p.Val880=
NM_001382787.1:c.2634C>A	NP_001369716.1:p.Val878=
NM_001382788.1:c.2589C>A	NP_001369717.1:p.Val863=
NM_001382789.1:c.2580C>A	NP_001369718.1:p.Val860=
NM_001382790.1:c.2556C>A	NP_001369719.1:p.Val852=
NM_001382791.1:c.2550C>A	NP_001369720.1:p.Val850=
NM_001382792.1:c.2523C>A	NP_001369721.1:p.Val841=
NM_001382793.1:c.2517C>A	NP_001369722.1:p.Val839=
NM_001382794.1:c.2517C>A	NP_001369723.1:p.Val839=
NM_001382795.1:c.2511C>A	NP_001369724.1:p.Val837=
NM_001382796.1:c.2559C>A	NP_001369725.1:p.Val853=
NM_001382797.1:c.2460C>A	NP_001369726.1:p.Val820=
NM_001382798.1:c.2493+203C>A	NP_001369727.1:n.2493+203C>A
NM_001382799.1:c.2379C>A	NP_001369728.1:p.Val793=
NM_001382800.1:c.2373C>A	NP_001369729.1:p.Val791=
NM_001382801.1:c.2445+203C>A	NP_001369730.1:n.2445+203C>A
NM_001382802.1:c.2301C>A	NP_001369731.1:p.Val767=
NM_001382803.1:c.2517C>A	NP_001369732.1:p.Val839=
NM_001382804.1:c.1731C>A	NP_001369733.1:p.Val577=
NM_001382805.1:c.2208+1454C>A	NP_001369734.1:n.2208+1454C>A
NM_001382806.1:c.1521C>A	NP_001369735.1:p.Val507=
NM_004448.4:c.2559C>A MANE Select	NP_004439.2:p.Val853=
NR_110535.2:n.2797C>A