Canonical Allele Identifier: CA399304672

Gene: ERBB2

Linked Data

• dbSNP Id: rs2145865309
• MyVariant Identifiers: chr17:g.37881383G>A (hg19) ; chr17:g.39725130G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39725130G>A , CM000679.2:g.39725130G>A	GRCh38
NC_000017.10:g.37881383G>A , CM000679.1:g.37881383G>A	GRCh37
NC_000017.9:g.35134909G>A	NCBI36
NG_007503.1:g.41991G>A , LRG_724:g.41991G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000269571.10:c.2575G>A MANE Select	ENSP00000269571.4:p.Val859Ile
ENST00000269571.9:c.2575G>A	ENSP00000269571.4:p.Val859Ile
ENST00000406381.6:c.2485G>A	ENSP00000385185.2:p.Val829Ile
ENST00000445658.6:c.1747G>A	ENSP00000404047.2:p.Val583Ile
ENST00000541774.5:c.2530G>A	ENSP00000446466.1:p.Val844Ile
ENST00000578373.5:c.*2365G>A	ENSP00000463427.1:n.*2365G>A
ENST00000580074.1:c.681G>A
ENST00000583038.5:n.3709G>A
ENST00000584450.5:c.2575G>A	ENSP00000463714.1:p.Val859Ile
ENST00000584601.5:c.2485G>A	ENSP00000462438.1:p.Val829Ile
NM_001005862.2:c.2485G>A , LRG_724t1:c.2485G>A	NP_001005862.1:p.Val829Ile
NM_001289936.1:c.2530G>A , LRG_724t4:c.2530G>A	NP_001276865.1:p.Val844Ile
NM_001289937.1:c.2575G>A	NP_001276866.1:p.Val859Ile
NM_004448.3:c.2575G>A , LRG_724t2:c.2575G>A	NP_004439.2:p.Val859Ile
NR_110535.1:n.2899G>A
XM_024450641.1:c.2713G>A	XP_024306409.1:p.Val905Ile
XM_024450642.1:c.2668G>A	XP_024306410.1:p.Val890Ile
XM_024450643.1:c.2623G>A	XP_024306411.1:p.Val875Ile
NM_001005862.3:c.2485G>A	NP_001005862.1:p.Val829Ile
NM_001289936.2:c.2530G>A	NP_001276865.1:p.Val844Ile
NM_001289937.2:c.2575G>A	NP_001276866.1:p.Val859Ile
NM_001382782.1:c.2485G>A	NP_001369711.1:p.Val829Ile
NM_001382783.1:c.2485G>A	NP_001369712.1:p.Val829Ile
NM_001382784.1:c.2692G>A	NP_001369713.1:p.Val898Ile
NM_001382785.1:c.2677G>A	NP_001369714.1:p.Val893Ile
NM_001382786.1:c.2656G>A	NP_001369715.1:p.Val886Ile
NM_001382787.1:c.2650G>A	NP_001369716.1:p.Val884Ile
NM_001382788.1:c.2605G>A	NP_001369717.1:p.Val869Ile
NM_001382789.1:c.2596G>A	NP_001369718.1:p.Val866Ile
NM_001382790.1:c.2572G>A	NP_001369719.1:p.Val858Ile
NM_001382791.1:c.2566G>A	NP_001369720.1:p.Val856Ile
NM_001382792.1:c.2539G>A	NP_001369721.1:p.Val847Ile
NM_001382793.1:c.2533G>A	NP_001369722.1:p.Val845Ile
NM_001382794.1:c.2533G>A	NP_001369723.1:p.Val845Ile
NM_001382795.1:c.2527G>A	NP_001369724.1:p.Val843Ile
NM_001382796.1:c.2575G>A	NP_001369725.1:p.Val859Ile
NM_001382797.1:c.2476G>A	NP_001369726.1:p.Val826Ile
NM_001382798.1:c.2494-197G>A	NP_001369727.1:n.2494-197G>A
NM_001382799.1:c.2395G>A	NP_001369728.1:p.Val799Ile
NM_001382800.1:c.2389G>A	NP_001369729.1:p.Val797Ile
NM_001382801.1:c.2446-197G>A	NP_001369730.1:n.2446-197G>A
NM_001382802.1:c.2317G>A	NP_001369731.1:p.Val773Ile
NM_001382803.1:c.2533G>A	NP_001369732.1:p.Val845Ile
NM_001382804.1:c.1747G>A	NP_001369733.1:p.Val583Ile
NM_001382805.1:c.2208+1470G>A	NP_001369734.1:n.2208+1470G>A
NM_001382806.1:c.1537G>A	NP_001369735.1:p.Val513Ile
NM_004448.4:c.2575G>A MANE Select	NP_004439.2:p.Val859Ile
NR_110535.2:n.2813G>A