Canonical Allele Identifier: CA399313487

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143300985
• MyVariant Identifiers: chr17:g.37884077A>G (hg19) ; chr17:g.39727824A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727824A>G , CM000679.2:g.39727824A>G	GRCh38
NC_000017.10:g.37884077A>G , CM000679.1:g.37884077A>G	GRCh37
NC_000017.9:g.35137603A>G	NCBI36
NG_007503.1:g.44685A>G , LRG_724:g.44685A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3548A>G MANE Select	ENSP00000269571.4:p.Asp1183Gly
ENST00000269571.9:c.3548A>G	ENSP00000269571.4:p.Asp1183Gly
ENST00000406381.6:c.3458A>G	ENSP00000385185.2:p.Asp1153Gly
ENST00000445658.6:c.2720A>G	ENSP00000404047.2:p.Asp907Gly
ENST00000541774.5:c.3503A>G	ENSP00000446466.1:p.Asp1168Gly
ENST00000578373.5:c.*3338A>G	ENSP00000463427.1:n.*3338A>G
ENST00000584450.5:c.*127A>G	ENSP00000463714.1:n.*127A>G
ENST00000584601.5:c.3458A>G	ENSP00000462438.1:p.Asp1153Gly
NM_001005862.2:c.3458A>G , LRG_724t1:c.3458A>G	NP_001005862.1:p.Asp1153Gly
NM_001289936.1:c.3503A>G , LRG_724t4:c.3503A>G	NP_001276865.1:p.Asp1168Gly
NM_001289937.1:c.*127A>G	NP_001276866.1:n.*127A>G
NM_004448.3:c.3548A>G , LRG_724t2:c.3548A>G	NP_004439.2:p.Asp1183Gly
NR_110535.1:n.3872A>G
XM_024450641.1:c.3686A>G	XP_024306409.1:p.Asp1229Gly
XM_024450642.1:c.3641A>G	XP_024306410.1:p.Asp1214Gly
XM_024450643.1:c.3596A>G	XP_024306411.1:p.Asp1199Gly
NM_001005862.3:c.3458A>G	NP_001005862.1:p.Asp1153Gly
NM_001289936.2:c.3503A>G	NP_001276865.1:p.Asp1168Gly
NM_001289937.2:c.*127A>G	NP_001276866.1:n.*127A>G
NM_001382782.1:c.3458A>G	NP_001369711.1:p.Asp1153Gly
NM_001382783.1:c.3458A>G	NP_001369712.1:p.Asp1153Gly
NM_001382784.1:c.3665A>G	NP_001369713.1:p.Asp1222Gly
NM_001382785.1:c.3650A>G	NP_001369714.1:p.Asp1217Gly
NM_001382786.1:c.3629A>G	NP_001369715.1:p.Asp1210Gly
NM_001382787.1:c.3623A>G	NP_001369716.1:p.Asp1208Gly
NM_001382788.1:c.3578A>G	NP_001369717.1:p.Asp1193Gly
NM_001382789.1:c.3569A>G	NP_001369718.1:p.Asp1190Gly
NM_001382790.1:c.3545A>G	NP_001369719.1:p.Asp1182Gly
NM_001382791.1:c.3539A>G	NP_001369720.1:p.Asp1180Gly
NM_001382792.1:c.3512A>G	NP_001369721.1:p.Asp1171Gly
NM_001382793.1:c.3506A>G	NP_001369722.1:p.Asp1169Gly
NM_001382794.1:c.3506A>G	NP_001369723.1:p.Asp1169Gly
NM_001382795.1:c.3500A>G	NP_001369724.1:p.Asp1167Gly
NM_001382796.1:c.3461A>G	NP_001369725.1:p.Asp1154Gly
NM_001382797.1:c.3449A>G	NP_001369726.1:p.Asp1150Gly
NM_001382798.1:c.3392A>G	NP_001369727.1:p.Asp1131Gly
NM_001382799.1:c.3368A>G	NP_001369728.1:p.Asp1123Gly
NM_001382800.1:c.3362A>G	NP_001369729.1:p.Asp1121Gly
NM_001382801.1:c.3344A>G	NP_001369730.1:p.Asp1115Gly
NM_001382802.1:c.3290A>G	NP_001369731.1:p.Asp1097Gly
NM_001382803.1:c.*127A>G	NP_001369732.1:n.*127A>G
NM_001382804.1:c.2720A>G	NP_001369733.1:p.Asp907Gly
NM_001382805.1:c.2597A>G	NP_001369734.1:p.Asp866Gly
NM_001382806.1:c.2510A>G	NP_001369735.1:p.Asp837Gly
NM_004448.4:c.3548A>G MANE Select	NP_004439.2:p.Asp1183Gly
NR_110535.2:n.3786A>G