Canonical Allele Identifier: CA399313131

Gene: ERBB2

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3497C>G MANE Select	ENSP00000269571.4:p.Thr1166Ser
ENST00000269571.9:c.3497C>G	ENSP00000269571.4:p.Thr1166Ser
ENST00000406381.6:c.3407C>G	ENSP00000385185.2:p.Thr1136Ser
ENST00000445658.6:c.2669C>G	ENSP00000404047.2:p.Thr890Ser
ENST00000541774.5:c.3452C>G	ENSP00000446466.1:p.Thr1151Ser
ENST00000578373.5:c.*3287C>G	ENSP00000463427.1:n.*3287C>G
ENST00000584450.5:c.*76C>G	ENSP00000463714.1:n.*76C>G
ENST00000584601.5:c.3407C>G	ENSP00000462438.1:p.Thr1136Ser
NM_001005862.2:c.3407C>G , LRG_724t1:c.3407C>G	NP_001005862.1:p.Thr1136Ser
NM_001289936.1:c.3452C>G , LRG_724t4:c.3452C>G	NP_001276865.1:p.Thr1151Ser
NM_001289937.1:c.*76C>G	NP_001276866.1:n.*76C>G
NM_004448.3:c.3497C>G , LRG_724t2:c.3497C>G	NP_004439.2:p.Thr1166Ser
NR_110535.1:n.3821C>G
XM_024450641.1:c.3635C>G	XP_024306409.1:p.Thr1212Ser
XM_024450642.1:c.3590C>G	XP_024306410.1:p.Thr1197Ser
XM_024450643.1:c.3545C>G	XP_024306411.1:p.Thr1182Ser
NM_001005862.3:c.3407C>G	NP_001005862.1:p.Thr1136Ser
NM_001289936.2:c.3452C>G	NP_001276865.1:p.Thr1151Ser
NM_001289937.2:c.*76C>G	NP_001276866.1:n.*76C>G
NM_001382782.1:c.3407C>G	NP_001369711.1:p.Thr1136Ser
NM_001382783.1:c.3407C>G	NP_001369712.1:p.Thr1136Ser
NM_001382784.1:c.3614C>G	NP_001369713.1:p.Thr1205Ser
NM_001382785.1:c.3599C>G	NP_001369714.1:p.Thr1200Ser
NM_001382786.1:c.3578C>G	NP_001369715.1:p.Thr1193Ser
NM_001382787.1:c.3572C>G	NP_001369716.1:p.Thr1191Ser
NM_001382788.1:c.3527C>G	NP_001369717.1:p.Thr1176Ser
NM_001382789.1:c.3518C>G	NP_001369718.1:p.Thr1173Ser
NM_001382790.1:c.3494C>G	NP_001369719.1:p.Thr1165Ser
NM_001382791.1:c.3488C>G	NP_001369720.1:p.Thr1163Ser
NM_001382792.1:c.3461C>G	NP_001369721.1:p.Thr1154Ser
NM_001382793.1:c.3455C>G	NP_001369722.1:p.Thr1152Ser
NM_001382794.1:c.3455C>G	NP_001369723.1:p.Thr1152Ser
NM_001382795.1:c.3449C>G	NP_001369724.1:p.Thr1150Ser
NM_001382796.1:c.3410C>G	NP_001369725.1:p.Thr1137Ser
NM_001382797.1:c.3398C>G	NP_001369726.1:p.Thr1133Ser
NM_001382798.1:c.3341C>G	NP_001369727.1:p.Thr1114Ser
NM_001382799.1:c.3317C>G	NP_001369728.1:p.Thr1106Ser
NM_001382800.1:c.3311C>G	NP_001369729.1:p.Thr1104Ser
NM_001382801.1:c.3293C>G	NP_001369730.1:p.Thr1098Ser
NM_001382802.1:c.3239C>G	NP_001369731.1:p.Thr1080Ser
NM_001382803.1:c.*76C>G	NP_001369732.1:n.*76C>G
NM_001382804.1:c.2669C>G	NP_001369733.1:p.Thr890Ser
NM_001382805.1:c.2546C>G	NP_001369734.1:p.Thr849Ser
NM_001382806.1:c.2459C>G	NP_001369735.1:p.Thr820Ser
NM_004448.4:c.3497C>G MANE Select	NP_004439.2:p.Thr1166Ser
NR_110535.2:n.3735C>G