Canonical Allele Identifier: CA399312850

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37883955G>T (hg19) ; chr17:g.39727702G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727702G>T , CM000679.2:g.39727702G>T	GRCh38
NC_000017.10:g.37883955G>T , CM000679.1:g.37883955G>T	GRCh37
NC_000017.9:g.35137481G>T	NCBI36
NG_007503.1:g.44563G>T , LRG_724:g.44563G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3426G>T MANE Select	ENSP00000269571.4:p.Gln1142His
ENST00000269571.9:c.3426G>T	ENSP00000269571.4:p.Gln1142His
ENST00000406381.6:c.3336G>T	ENSP00000385185.2:p.Gln1112His
ENST00000445658.6:c.2598G>T	ENSP00000404047.2:p.Gln866His
ENST00000541774.5:c.3381G>T	ENSP00000446466.1:p.Gln1127His
ENST00000578373.5:c.*3216G>T	ENSP00000463427.1:n.*3216G>T
ENST00000584450.5:c.*5G>T	ENSP00000463714.1:n.*5G>T
ENST00000584601.5:c.3336G>T	ENSP00000462438.1:p.Gln1112His
NM_001005862.2:c.3336G>T , LRG_724t1:c.3336G>T	NP_001005862.1:p.Gln1112His
NM_001289936.1:c.3381G>T , LRG_724t4:c.3381G>T	NP_001276865.1:p.Gln1127His
NM_001289937.1:c.*5G>T	NP_001276866.1:n.*5G>T
NM_004448.3:c.3426G>T , LRG_724t2:c.3426G>T	NP_004439.2:p.Gln1142His
NR_110535.1:n.3750G>T
XM_024450641.1:c.3564G>T	XP_024306409.1:p.Gln1188His
XM_024450642.1:c.3519G>T	XP_024306410.1:p.Gln1173His
XM_024450643.1:c.3474G>T	XP_024306411.1:p.Gln1158His
NM_001005862.3:c.3336G>T	NP_001005862.1:p.Gln1112His
NM_001289936.2:c.3381G>T	NP_001276865.1:p.Gln1127His
NM_001289937.2:c.*5G>T	NP_001276866.1:n.*5G>T
NM_001382782.1:c.3336G>T	NP_001369711.1:p.Gln1112His
NM_001382783.1:c.3336G>T	NP_001369712.1:p.Gln1112His
NM_001382784.1:c.3543G>T	NP_001369713.1:p.Gln1181His
NM_001382785.1:c.3528G>T	NP_001369714.1:p.Gln1176His
NM_001382786.1:c.3507G>T	NP_001369715.1:p.Gln1169His
NM_001382787.1:c.3501G>T	NP_001369716.1:p.Gln1167His
NM_001382788.1:c.3456G>T	NP_001369717.1:p.Gln1152His
NM_001382789.1:c.3447G>T	NP_001369718.1:p.Gln1149His
NM_001382790.1:c.3423G>T	NP_001369719.1:p.Gln1141His
NM_001382791.1:c.3417G>T	NP_001369720.1:p.Gln1139His
NM_001382792.1:c.3390G>T	NP_001369721.1:p.Gln1130His
NM_001382793.1:c.3384G>T	NP_001369722.1:p.Gln1128His
NM_001382794.1:c.3384G>T	NP_001369723.1:p.Gln1128His
NM_001382795.1:c.3378G>T	NP_001369724.1:p.Gln1126His
NM_001382796.1:c.3339G>T	NP_001369725.1:p.Gln1113His
NM_001382797.1:c.3327G>T	NP_001369726.1:p.Gln1109His
NM_001382798.1:c.3270G>T	NP_001369727.1:p.Gln1090His
NM_001382799.1:c.3246G>T	NP_001369728.1:p.Gln1082His
NM_001382800.1:c.3240G>T	NP_001369729.1:p.Gln1080His
NM_001382801.1:c.3222G>T	NP_001369730.1:p.Gln1074His
NM_001382802.1:c.3168G>T	NP_001369731.1:p.Gln1056His
NM_001382803.1:c.*5G>T	NP_001369732.1:n.*5G>T
NM_001382804.1:c.2598G>T	NP_001369733.1:p.Gln866His
NM_001382805.1:c.2475G>T	NP_001369734.1:p.Gln825His
NM_001382806.1:c.2388G>T	NP_001369735.1:p.Gln796His
NM_004448.4:c.3426G>T MANE Select	NP_004439.2:p.Gln1142His
NR_110535.2:n.3664G>T