Canonical Allele Identifier: CA399312796

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143261474
• MyVariant Identifiers: chr17:g.37883796G>T (hg19) ; chr17:g.39727543G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727543G>T , CM000679.2:g.39727543G>T	GRCh38
NC_000017.10:g.37883796G>T , CM000679.1:g.37883796G>T	GRCh37
NC_000017.9:g.35137322G>T	NCBI36
NG_007503.1:g.44404G>T , LRG_724:g.44404G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3408G>T MANE Select	ENSP00000269571.4:p.Gln1136His
ENST00000269571.9:c.3408G>T	ENSP00000269571.4:p.Gln1136His
ENST00000406381.6:c.3318G>T	ENSP00000385185.2:p.Gln1106His
ENST00000445658.6:c.2580G>T	ENSP00000404047.2:p.Gln860His
ENST00000541774.5:c.3363G>T	ENSP00000446466.1:p.Gln1121His
ENST00000578373.5:c.*3198G>T	ENSP00000463427.1:n.*3198G>T
ENST00000584450.5:c.3160-146G>T	ENSP00000463714.1:n.3160-146G>T
ENST00000584601.5:c.3318G>T	ENSP00000462438.1:p.Gln1106His
NM_001005862.2:c.3318G>T , LRG_724t1:c.3318G>T	NP_001005862.1:p.Gln1106His
NM_001289936.1:c.3363G>T , LRG_724t4:c.3363G>T	NP_001276865.1:p.Gln1121His
NM_001289937.1:c.3160-146G>T	NP_001276866.1:n.3160-146G>T
NM_004448.3:c.3408G>T , LRG_724t2:c.3408G>T	NP_004439.2:p.Gln1136His
NR_110535.1:n.3732G>T
XM_024450641.1:c.3546G>T	XP_024306409.1:p.Gln1182His
XM_024450642.1:c.3501G>T	XP_024306410.1:p.Gln1167His
XM_024450643.1:c.3456G>T	XP_024306411.1:p.Gln1152His
NM_001005862.3:c.3318G>T	NP_001005862.1:p.Gln1106His
NM_001289936.2:c.3363G>T	NP_001276865.1:p.Gln1121His
NM_001289937.2:c.3160-146G>T	NP_001276866.1:n.3160-146G>T
NM_001382782.1:c.3318G>T	NP_001369711.1:p.Gln1106His
NM_001382783.1:c.3318G>T	NP_001369712.1:p.Gln1106His
NM_001382784.1:c.3525G>T	NP_001369713.1:p.Gln1175His
NM_001382785.1:c.3510G>T	NP_001369714.1:p.Gln1170His
NM_001382786.1:c.3489G>T	NP_001369715.1:p.Gln1163His
NM_001382787.1:c.3483G>T	NP_001369716.1:p.Gln1161His
NM_001382788.1:c.3438G>T	NP_001369717.1:p.Gln1146His
NM_001382789.1:c.3429G>T	NP_001369718.1:p.Gln1143His
NM_001382790.1:c.3405G>T	NP_001369719.1:p.Gln1135His
NM_001382791.1:c.3399G>T	NP_001369720.1:p.Gln1133His
NM_001382792.1:c.3372G>T	NP_001369721.1:p.Gln1124His
NM_001382793.1:c.3366G>T	NP_001369722.1:p.Gln1122His
NM_001382794.1:c.3366G>T	NP_001369723.1:p.Gln1122His
NM_001382795.1:c.3360G>T	NP_001369724.1:p.Gln1120His
NM_001382796.1:c.3321G>T	NP_001369725.1:p.Gln1107His
NM_001382797.1:c.3309G>T	NP_001369726.1:p.Gln1103His
NM_001382798.1:c.3252G>T	NP_001369727.1:p.Gln1084His
NM_001382799.1:c.3228G>T	NP_001369728.1:p.Gln1076His
NM_001382800.1:c.3222G>T	NP_001369729.1:p.Gln1074His
NM_001382801.1:c.3204G>T	NP_001369730.1:p.Gln1068His
NM_001382802.1:c.3150G>T	NP_001369731.1:p.Gln1050His
NM_001382803.1:c.3118-146G>T	NP_001369732.1:n.3118-146G>T
NM_001382804.1:c.2580G>T	NP_001369733.1:p.Gln860His
NM_001382805.1:c.2457G>T	NP_001369734.1:p.Gln819His
NM_001382806.1:c.2370G>T	NP_001369735.1:p.Gln790His
NM_004448.4:c.3408G>T MANE Select	NP_004439.2:p.Gln1136His
NR_110535.2:n.3646G>T