Canonical Allele Identifier: CA399303307

Gene: ERBB2

Linked Data

• dbSNP Id: rs2145850831
• MyVariant Identifiers: chr17:g.37881075C>A (hg19) ; chr17:g.39724822C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39724822C>A , CM000679.2:g.39724822C>A	GRCh38
NC_000017.10:g.37881075C>A , CM000679.1:g.37881075C>A	GRCh37
NC_000017.9:g.35134601C>A	NCBI36
NG_007503.1:g.41683C>A , LRG_724:g.41683C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.2404C>A MANE Select	ENSP00000269571.4:p.Pro802Thr
ENST00000269571.9:c.2404C>A	ENSP00000269571.4:p.Pro802Thr
ENST00000406381.6:c.2314C>A	ENSP00000385185.2:p.Pro772Thr
ENST00000445658.6:c.1576C>A	ENSP00000404047.2:p.Pro526Thr
ENST00000541774.5:c.2359C>A	ENSP00000446466.1:p.Pro787Thr
ENST00000578373.5:c.*2194C>A	ENSP00000463427.1:n.*2194C>A
ENST00000580074.1:c.510C>A
ENST00000583038.5:n.3538C>A
ENST00000584450.5:c.2404C>A	ENSP00000463714.1:p.Pro802Thr
ENST00000584601.5:c.2314C>A	ENSP00000462438.1:p.Pro772Thr
NM_001005862.2:c.2314C>A , LRG_724t1:c.2314C>A	NP_001005862.1:p.Pro772Thr
NM_001289936.1:c.2359C>A , LRG_724t4:c.2359C>A	NP_001276865.1:p.Pro787Thr
NM_001289937.1:c.2404C>A	NP_001276866.1:p.Pro802Thr
NM_004448.3:c.2404C>A , LRG_724t2:c.2404C>A	NP_004439.2:p.Pro802Thr
NR_110535.1:n.2728C>A
XM_024450641.1:c.2542C>A	XP_024306409.1:p.Pro848Thr
XM_024450642.1:c.2497C>A	XP_024306410.1:p.Pro833Thr
XM_024450643.1:c.2452C>A	XP_024306411.1:p.Pro818Thr
NM_001005862.3:c.2314C>A	NP_001005862.1:p.Pro772Thr
NM_001289936.2:c.2359C>A	NP_001276865.1:p.Pro787Thr
NM_001289937.2:c.2404C>A	NP_001276866.1:p.Pro802Thr
NM_001382782.1:c.2314C>A	NP_001369711.1:p.Pro772Thr
NM_001382783.1:c.2314C>A	NP_001369712.1:p.Pro772Thr
NM_001382784.1:c.2521C>A	NP_001369713.1:p.Pro841Thr
NM_001382785.1:c.2506C>A	NP_001369714.1:p.Pro836Thr
NM_001382786.1:c.2485C>A	NP_001369715.1:p.Pro829Thr
NM_001382787.1:c.2479C>A	NP_001369716.1:p.Pro827Thr
NM_001382788.1:c.2434C>A	NP_001369717.1:p.Pro812Thr
NM_001382789.1:c.2425C>A	NP_001369718.1:p.Pro809Thr
NM_001382790.1:c.2401C>A	NP_001369719.1:p.Pro801Thr
NM_001382791.1:c.2395C>A	NP_001369720.1:p.Pro799Thr
NM_001382792.1:c.2368C>A	NP_001369721.1:p.Pro790Thr
NM_001382793.1:c.2362C>A	NP_001369722.1:p.Pro788Thr
NM_001382794.1:c.2362C>A	NP_001369723.1:p.Pro788Thr
NM_001382795.1:c.2356C>A	NP_001369724.1:p.Pro786Thr
NM_001382796.1:c.2404C>A	NP_001369725.1:p.Pro802Thr
NM_001382797.1:c.2305C>A	NP_001369726.1:p.Pro769Thr
NM_001382798.1:c.2404C>A	NP_001369727.1:p.Pro802Thr
NM_001382799.1:c.2224C>A	NP_001369728.1:p.Pro742Thr
NM_001382800.1:c.2308-227C>A	NP_001369729.1:n.2308-227C>A
NM_001382801.1:c.2356C>A	NP_001369730.1:p.Pro786Thr
NM_001382802.1:c.2146C>A	NP_001369731.1:p.Pro716Thr
NM_001382803.1:c.2362C>A	NP_001369732.1:p.Pro788Thr
NM_001382804.1:c.1576C>A	NP_001369733.1:p.Pro526Thr
NM_001382805.1:c.2208+1162C>A	NP_001369734.1:n.2208+1162C>A
NM_001382806.1:c.1366C>A	NP_001369735.1:p.Pro456Thr
NM_004448.4:c.2404C>A MANE Select	NP_004439.2:p.Pro802Thr
NR_110535.2:n.2642C>A