Canonical Allele Identifier: CA399304721

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37881389A>T (hg19) ; chr17:g.39725136A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39725136A>T , CM000679.2:g.39725136A>T	GRCh38
NC_000017.10:g.37881389A>T , CM000679.1:g.37881389A>T	GRCh37
NC_000017.9:g.35134915A>T	NCBI36
NG_007503.1:g.41997A>T , LRG_724:g.41997A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000269571.10:c.2581A>T MANE Select	ENSP00000269571.4:p.Ile861Phe
ENST00000269571.9:c.2581A>T	ENSP00000269571.4:p.Ile861Phe
ENST00000406381.6:c.2491A>T	ENSP00000385185.2:p.Ile831Phe
ENST00000445658.6:c.1753A>T	ENSP00000404047.2:p.Ile585Phe
ENST00000541774.5:c.2536A>T	ENSP00000446466.1:p.Ile846Phe
ENST00000578373.5:c.*2371A>T	ENSP00000463427.1:n.*2371A>T
ENST00000580074.1:c.687A>T
ENST00000583038.5:n.3715A>T
ENST00000584450.5:c.2581A>T	ENSP00000463714.1:p.Ile861Phe
ENST00000584601.5:c.2491A>T	ENSP00000462438.1:p.Ile831Phe
NM_001005862.2:c.2491A>T , LRG_724t1:c.2491A>T	NP_001005862.1:p.Ile831Phe
NM_001289936.1:c.2536A>T , LRG_724t4:c.2536A>T	NP_001276865.1:p.Ile846Phe
NM_001289937.1:c.2581A>T	NP_001276866.1:p.Ile861Phe
NM_004448.3:c.2581A>T , LRG_724t2:c.2581A>T	NP_004439.2:p.Ile861Phe
NR_110535.1:n.2905A>T
XM_024450641.1:c.2719A>T	XP_024306409.1:p.Ile907Phe
XM_024450642.1:c.2674A>T	XP_024306410.1:p.Ile892Phe
XM_024450643.1:c.2629A>T	XP_024306411.1:p.Ile877Phe
NM_001005862.3:c.2491A>T	NP_001005862.1:p.Ile831Phe
NM_001289936.2:c.2536A>T	NP_001276865.1:p.Ile846Phe
NM_001289937.2:c.2581A>T	NP_001276866.1:p.Ile861Phe
NM_001382782.1:c.2491A>T	NP_001369711.1:p.Ile831Phe
NM_001382783.1:c.2491A>T	NP_001369712.1:p.Ile831Phe
NM_001382784.1:c.2698A>T	NP_001369713.1:p.Ile900Phe
NM_001382785.1:c.2683A>T	NP_001369714.1:p.Ile895Phe
NM_001382786.1:c.2662A>T	NP_001369715.1:p.Ile888Phe
NM_001382787.1:c.2656A>T	NP_001369716.1:p.Ile886Phe
NM_001382788.1:c.2611A>T	NP_001369717.1:p.Ile871Phe
NM_001382789.1:c.2602A>T	NP_001369718.1:p.Ile868Phe
NM_001382790.1:c.2578A>T	NP_001369719.1:p.Ile860Phe
NM_001382791.1:c.2572A>T	NP_001369720.1:p.Ile858Phe
NM_001382792.1:c.2545A>T	NP_001369721.1:p.Ile849Phe
NM_001382793.1:c.2539A>T	NP_001369722.1:p.Ile847Phe
NM_001382794.1:c.2539A>T	NP_001369723.1:p.Ile847Phe
NM_001382795.1:c.2533A>T	NP_001369724.1:p.Ile845Phe
NM_001382796.1:c.2581A>T	NP_001369725.1:p.Ile861Phe
NM_001382797.1:c.2482A>T	NP_001369726.1:p.Ile828Phe
NM_001382798.1:c.2494-191A>T	NP_001369727.1:n.2494-191A>T
NM_001382799.1:c.2401A>T	NP_001369728.1:p.Ile801Phe
NM_001382800.1:c.2395A>T	NP_001369729.1:p.Ile799Phe
NM_001382801.1:c.2446-191A>T	NP_001369730.1:n.2446-191A>T
NM_001382802.1:c.2323A>T	NP_001369731.1:p.Ile775Phe
NM_001382803.1:c.2539A>T	NP_001369732.1:p.Ile847Phe
NM_001382804.1:c.1753A>T	NP_001369733.1:p.Ile585Phe
NM_001382805.1:c.2208+1476A>T	NP_001369734.1:n.2208+1476A>T
NM_001382806.1:c.1543A>T	NP_001369735.1:p.Ile515Phe
NM_004448.4:c.2581A>T MANE Select	NP_004439.2:p.Ile861Phe
NR_110535.2:n.2819A>T