Canonical Allele Identifier: CA499670900

Gene: ERBB2

Linked Data

• dbSNP Id: rs2059659401
• MyVariant Identifiers: chr17:g.37881077C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39724824C>T , CM000679.2:g.39724824C>T	GRCh38
NC_000017.10:g.37881077C>T , CM000679.1:g.37881077C>T	GRCh37
NC_000017.9:g.35134603C>T	NCBI36
NG_007503.1:g.41685C>T , LRG_724:g.41685C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.2406C>T MANE Select	ENSP00000269571.4:p.Pro802=
ENST00000269571.9:c.2406C>T	ENSP00000269571.4:p.Pro802=
ENST00000406381.6:c.2316C>T	ENSP00000385185.2:p.Pro772=
ENST00000445658.6:c.1578C>T	ENSP00000404047.2:p.Pro526=
ENST00000541774.5:c.2361C>T	ENSP00000446466.1:p.Pro787=
ENST00000578373.5:c.*2196C>T	ENSP00000463427.1:n.*2196C>T
ENST00000580074.1:c.512C>T
ENST00000583038.5:n.3540C>T
ENST00000584450.5:c.2406C>T	ENSP00000463714.1:p.Pro802=
ENST00000584601.5:c.2316C>T	ENSP00000462438.1:p.Pro772=
NM_001005862.2:c.2316C>T , LRG_724t1:c.2316C>T	NP_001005862.1:p.Pro772=
NM_001289936.1:c.2361C>T , LRG_724t4:c.2361C>T	NP_001276865.1:p.Pro787=
NM_001289937.1:c.2406C>T	NP_001276866.1:p.Pro802=
NM_004448.3:c.2406C>T , LRG_724t2:c.2406C>T	NP_004439.2:p.Pro802=
NR_110535.1:n.2730C>T
XM_024450641.1:c.2544C>T	XP_024306409.1:p.Pro848=
XM_024450642.1:c.2499C>T	XP_024306410.1:p.Pro833=
XM_024450643.1:c.2454C>T	XP_024306411.1:p.Pro818=
NM_001005862.3:c.2316C>T	NP_001005862.1:p.Pro772=
NM_001289936.2:c.2361C>T	NP_001276865.1:p.Pro787=
NM_001289937.2:c.2406C>T	NP_001276866.1:p.Pro802=
NM_001382782.1:c.2316C>T	NP_001369711.1:p.Pro772=
NM_001382783.1:c.2316C>T	NP_001369712.1:p.Pro772=
NM_001382784.1:c.2523C>T	NP_001369713.1:p.Pro841=
NM_001382785.1:c.2508C>T	NP_001369714.1:p.Pro836=
NM_001382786.1:c.2487C>T	NP_001369715.1:p.Pro829=
NM_001382787.1:c.2481C>T	NP_001369716.1:p.Pro827=
NM_001382788.1:c.2436C>T	NP_001369717.1:p.Pro812=
NM_001382789.1:c.2427C>T	NP_001369718.1:p.Pro809=
NM_001382790.1:c.2403C>T	NP_001369719.1:p.Pro801=
NM_001382791.1:c.2397C>T	NP_001369720.1:p.Pro799=
NM_001382792.1:c.2370C>T	NP_001369721.1:p.Pro790=
NM_001382793.1:c.2364C>T	NP_001369722.1:p.Pro788=
NM_001382794.1:c.2364C>T	NP_001369723.1:p.Pro788=
NM_001382795.1:c.2358C>T	NP_001369724.1:p.Pro786=
NM_001382796.1:c.2406C>T	NP_001369725.1:p.Pro802=
NM_001382797.1:c.2307C>T	NP_001369726.1:p.Pro769=
NM_001382798.1:c.2406C>T	NP_001369727.1:p.Pro802=
NM_001382799.1:c.2226C>T	NP_001369728.1:p.Pro742=
NM_001382800.1:c.2308-225C>T	NP_001369729.1:n.2308-225C>T
NM_001382801.1:c.2358C>T	NP_001369730.1:p.Pro786=
NM_001382802.1:c.2148C>T	NP_001369731.1:p.Pro716=
NM_001382803.1:c.2364C>T	NP_001369732.1:p.Pro788=
NM_001382804.1:c.1578C>T	NP_001369733.1:p.Pro526=
NM_001382805.1:c.2208+1164C>T	NP_001369734.1:n.2208+1164C>T
NM_001382806.1:c.1368C>T	NP_001369735.1:p.Pro456=
NM_004448.4:c.2406C>T MANE Select	NP_004439.2:p.Pro802=
NR_110535.2:n.2644C>T