Canonical Allele Identifier: CA499890119

Gene: ERBB2

Linked Data

• dbSNP Id: rs2145864071
• MyVariant Identifiers: chr17:g.37881352T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39725099T>A , CM000679.2:g.39725099T>A	GRCh38
NC_000017.10:g.37881352T>A , CM000679.1:g.37881352T>A	GRCh37
NC_000017.9:g.35134878T>A	NCBI36
NG_007503.1:g.41960T>A , LRG_724:g.41960T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.2544T>A MANE Select	ENSP00000269571.4:p.Ala848=
ENST00000269571.9:c.2544T>A	ENSP00000269571.4:p.Ala848=
ENST00000406381.6:c.2454T>A	ENSP00000385185.2:p.Ala818=
ENST00000445658.6:c.1716T>A	ENSP00000404047.2:p.Ala572=
ENST00000541774.5:c.2499T>A	ENSP00000446466.1:p.Ala833=
ENST00000578373.5:c.*2334T>A	ENSP00000463427.1:n.*2334T>A
ENST00000580074.1:c.650T>A
ENST00000583038.5:n.3678T>A
ENST00000584450.5:c.2544T>A	ENSP00000463714.1:p.Ala848=
ENST00000584601.5:c.2454T>A	ENSP00000462438.1:p.Ala818=
NM_001005862.2:c.2454T>A , LRG_724t1:c.2454T>A	NP_001005862.1:p.Ala818=
NM_001289936.1:c.2499T>A , LRG_724t4:c.2499T>A	NP_001276865.1:p.Ala833=
NM_001289937.1:c.2544T>A	NP_001276866.1:p.Ala848=
NM_004448.3:c.2544T>A , LRG_724t2:c.2544T>A	NP_004439.2:p.Ala848=
NR_110535.1:n.2868T>A
XM_024450641.1:c.2682T>A	XP_024306409.1:p.Ala894=
XM_024450642.1:c.2637T>A	XP_024306410.1:p.Ala879=
XM_024450643.1:c.2592T>A	XP_024306411.1:p.Ala864=
NM_001005862.3:c.2454T>A	NP_001005862.1:p.Ala818=
NM_001289936.2:c.2499T>A	NP_001276865.1:p.Ala833=
NM_001289937.2:c.2544T>A	NP_001276866.1:p.Ala848=
NM_001382782.1:c.2454T>A	NP_001369711.1:p.Ala818=
NM_001382783.1:c.2454T>A	NP_001369712.1:p.Ala818=
NM_001382784.1:c.2661T>A	NP_001369713.1:p.Ala887=
NM_001382785.1:c.2646T>A	NP_001369714.1:p.Ala882=
NM_001382786.1:c.2625T>A	NP_001369715.1:p.Ala875=
NM_001382787.1:c.2619T>A	NP_001369716.1:p.Ala873=
NM_001382788.1:c.2574T>A	NP_001369717.1:p.Ala858=
NM_001382789.1:c.2565T>A	NP_001369718.1:p.Ala855=
NM_001382790.1:c.2541T>A	NP_001369719.1:p.Ala847=
NM_001382791.1:c.2535T>A	NP_001369720.1:p.Ala845=
NM_001382792.1:c.2508T>A	NP_001369721.1:p.Ala836=
NM_001382793.1:c.2502T>A	NP_001369722.1:p.Ala834=
NM_001382794.1:c.2502T>A	NP_001369723.1:p.Ala834=
NM_001382795.1:c.2496T>A	NP_001369724.1:p.Ala832=
NM_001382796.1:c.2544T>A	NP_001369725.1:p.Ala848=
NM_001382797.1:c.2445T>A	NP_001369726.1:p.Ala815=
NM_001382798.1:c.2493+188T>A	NP_001369727.1:n.2493+188T>A
NM_001382799.1:c.2364T>A	NP_001369728.1:p.Ala788=
NM_001382800.1:c.2358T>A	NP_001369729.1:p.Ala786=
NM_001382801.1:c.2445+188T>A	NP_001369730.1:n.2445+188T>A
NM_001382802.1:c.2286T>A	NP_001369731.1:p.Ala762=
NM_001382803.1:c.2502T>A	NP_001369732.1:p.Ala834=
NM_001382804.1:c.1716T>A	NP_001369733.1:p.Ala572=
NM_001382805.1:c.2208+1439T>A	NP_001369734.1:n.2208+1439T>A
NM_001382806.1:c.1506T>A	NP_001369735.1:p.Ala502=
NM_004448.4:c.2544T>A MANE Select	NP_004439.2:p.Ala848=
NR_110535.2:n.2782T>A