Canonical Allele Identifier: CA399313133

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143295291
• MyVariant Identifiers: chr17:g.37884026C>T (hg19) ; chr17:g.39727773C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727773C>T , CM000679.2:g.39727773C>T	GRCh38
NC_000017.10:g.37884026C>T , CM000679.1:g.37884026C>T	GRCh37
NC_000017.9:g.35137552C>T	NCBI36
NG_007503.1:g.44634C>T , LRG_724:g.44634C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3497C>T MANE Select	ENSP00000269571.4:p.Thr1166Ile
ENST00000269571.9:c.3497C>T	ENSP00000269571.4:p.Thr1166Ile
ENST00000406381.6:c.3407C>T	ENSP00000385185.2:p.Thr1136Ile
ENST00000445658.6:c.2669C>T	ENSP00000404047.2:p.Thr890Ile
ENST00000541774.5:c.3452C>T	ENSP00000446466.1:p.Thr1151Ile
ENST00000578373.5:c.*3287C>T	ENSP00000463427.1:n.*3287C>T
ENST00000584450.5:c.*76C>T	ENSP00000463714.1:n.*76C>T
ENST00000584601.5:c.3407C>T	ENSP00000462438.1:p.Thr1136Ile
NM_001005862.2:c.3407C>T , LRG_724t1:c.3407C>T	NP_001005862.1:p.Thr1136Ile
NM_001289936.1:c.3452C>T , LRG_724t4:c.3452C>T	NP_001276865.1:p.Thr1151Ile
NM_001289937.1:c.*76C>T	NP_001276866.1:n.*76C>T
NM_004448.3:c.3497C>T , LRG_724t2:c.3497C>T	NP_004439.2:p.Thr1166Ile
NR_110535.1:n.3821C>T
XM_024450641.1:c.3635C>T	XP_024306409.1:p.Thr1212Ile
XM_024450642.1:c.3590C>T	XP_024306410.1:p.Thr1197Ile
XM_024450643.1:c.3545C>T	XP_024306411.1:p.Thr1182Ile
NM_001005862.3:c.3407C>T	NP_001005862.1:p.Thr1136Ile
NM_001289936.2:c.3452C>T	NP_001276865.1:p.Thr1151Ile
NM_001289937.2:c.*76C>T	NP_001276866.1:n.*76C>T
NM_001382782.1:c.3407C>T	NP_001369711.1:p.Thr1136Ile
NM_001382783.1:c.3407C>T	NP_001369712.1:p.Thr1136Ile
NM_001382784.1:c.3614C>T	NP_001369713.1:p.Thr1205Ile
NM_001382785.1:c.3599C>T	NP_001369714.1:p.Thr1200Ile
NM_001382786.1:c.3578C>T	NP_001369715.1:p.Thr1193Ile
NM_001382787.1:c.3572C>T	NP_001369716.1:p.Thr1191Ile
NM_001382788.1:c.3527C>T	NP_001369717.1:p.Thr1176Ile
NM_001382789.1:c.3518C>T	NP_001369718.1:p.Thr1173Ile
NM_001382790.1:c.3494C>T	NP_001369719.1:p.Thr1165Ile
NM_001382791.1:c.3488C>T	NP_001369720.1:p.Thr1163Ile
NM_001382792.1:c.3461C>T	NP_001369721.1:p.Thr1154Ile
NM_001382793.1:c.3455C>T	NP_001369722.1:p.Thr1152Ile
NM_001382794.1:c.3455C>T	NP_001369723.1:p.Thr1152Ile
NM_001382795.1:c.3449C>T	NP_001369724.1:p.Thr1150Ile
NM_001382796.1:c.3410C>T	NP_001369725.1:p.Thr1137Ile
NM_001382797.1:c.3398C>T	NP_001369726.1:p.Thr1133Ile
NM_001382798.1:c.3341C>T	NP_001369727.1:p.Thr1114Ile
NM_001382799.1:c.3317C>T	NP_001369728.1:p.Thr1106Ile
NM_001382800.1:c.3311C>T	NP_001369729.1:p.Thr1104Ile
NM_001382801.1:c.3293C>T	NP_001369730.1:p.Thr1098Ile
NM_001382802.1:c.3239C>T	NP_001369731.1:p.Thr1080Ile
NM_001382803.1:c.*76C>T	NP_001369732.1:n.*76C>T
NM_001382804.1:c.2669C>T	NP_001369733.1:p.Thr890Ile
NM_001382805.1:c.2546C>T	NP_001369734.1:p.Thr849Ile
NM_001382806.1:c.2459C>T	NP_001369735.1:p.Thr820Ile
NM_004448.4:c.3497C>T MANE Select	NP_004439.2:p.Thr1166Ile
NR_110535.2:n.3735C>T